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US2441491A - Cyanacetylamino phenol color formers for color photography - Google Patents

Cyanacetylamino phenol color formers for color photography Download PDF

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Publication number
US2441491A
US2441491A US591828A US59182845A US2441491A US 2441491 A US2441491 A US 2441491A US 591828 A US591828 A US 591828A US 59182845 A US59182845 A US 59182845A US 2441491 A US2441491 A US 2441491A
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colour
cyanacetylamino
color
group
phenol
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US591828A
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Kendall John David
Fry Douglas James
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Ilford Imaging UK Ltd
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Ilford Ltd
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/32Colour coupling substances

Definitions

  • This invention relates to colour photography and particularly to dyestuff intermediates for use in colour photographic processes.
  • colour-formers compounds, generally known as colour-formers" or colourcouplers, which couple with theoxidation products of such developers, formed during development, to form quinone-imine or azomethine dyes.
  • the colour-couplers may be present in the developing solution employed, or may be included in a photographic emulsion layer which contains the reducible silver salt image, or in an adjacent layer or a layer separated from the said emulsion layer only by a thin Water-permeable layer.
  • Thedeveloping agent may be, for example, p-phenylene diamine or its N.N.-dialkyl derivatives, e. g. N.N.-dimethyl and N.N.-diethyl p-ph'enylene diamines, or a homologue, e. g. 5-diethylamino-2- amino-toluene.
  • ja'process of colour photography comprises developing a reducible silver. salt image by means of an aro-v matic primary amino developing agent in the presence of a cyanaetylamino phenol of the general formula:
  • Such compounds may be prepared by reacting together an aminophenol (or naphthol or higher homologous compound) 'which is unsubstituted in' the para position tothe hydroxy group, or contains i a carboxyLsulphonic, halogen or other easily removable atom'or group in such position, with ethyl cyanacetate.
  • an aminophenol or naphthol or higher homologous compound
  • cyanacet-o-hydroxy-anilide may be prepared from o-amino-phenol and 'ethylcyanacetate in hot xylene solution in the presence of piperidine or other base. The'product separates on cooling, and after purification has a melting point of 178" 0.
  • amino phenols and ,amino naphthols which may be similarly employed as initial reagents .are; for example, m-amino-phenol, 3- amino-e-naphthol, ,2-amino-5-ethoxy phenol, 2- amino-3-methyl 'phenol and 2-amino-5-chlor ph'enol. 1
  • Particular compounds which may be employed arez' 1-cyanacetylamino-2ehydroxy-l-ethoxy benzene 2-cyan'acetylamino l-hydroxy naphthalene I-cyanacetyIaminO-2-hydroxy-6-methyl benzene These compounds are made by the general process described above, using the appropriate reagents.
  • the benzene, naphthalene or other ring system present may'contain other substituent groups, e; g. hydrocarbon groups or alkoxy groups.
  • the colour-couplers of this invention maybe included in a developing solution containin an aromatic primary amino developing agent, or may be included in a silver halide emulsion layer, or in a water-permeable colloid layer coated next to a silver halide emulsion layer, or separated therefrom only by a thin water-permeable layer.
  • the colour-couplers of this invention may be used in any of the colour processes of U. S. Patents Nos. 2,350,380, 2,363,764 and 2,369,171 and British Patents Nos. 551,116, 551,117, 554,302 and 556,858.
  • the formation of coloured images by means of the colour-couplers of this invention may be applied to the development of a reducible silver salt image which is an original latent image formed in the emulsion layer by exposure to light, or which is an image obtained by the conversion of a silver image to areducible silver salt i a e by the usual ble hin techni ue;
  • colour photographic processes in which the dye is formed by the coupling of the colourcouplers of the invention with the endatienprednets of an aromatic primary amino developing agent formed in situ during the deyeiopment, of a reducible silver salt image, ;th'e colours-couplers of the invention may also be employed in other colour photographic processes, ,e, g, .processesin which the dye is formed by direct coupling between the colour-coupler and a nitroso aniline, e. g. penitroso dialkyl aniline, or between the colour-coupler and a diazo compound.
  • a nitroso aniline e. g. penitroso dialkyl aniline
  • opin age trermin an a omethi idyeimase .situ with t e dev lop dsi er ima e, the esidua o o ler c p d it .;.a diet-to compound ppl di ution, t the ph tos arms el ment and t e n l az meth ne .de image bleached out, eavi only he az .dyeuiinage n the layer.
  • a process of colour photography which comprises developing a reducible silver salt in a pho tographic element by means ore solution of an aromatic primary amino developing agent containing a compoundei t g neral o mu V NH.CO.CH2.CN
  • a photographic element for colour photography which comprises a support bearing at least one layer of a light-sensitive silver halide emulsign and, adjacent thereto, a layer containing a compound of the general formula:
  • hydroxy group is in a position taken frorn the group consisting of ortho and meta positions to the cyanacetylamino group and where X para to the hydroxy group and is a member selected from the class consisting .of the ydrogen 'andhalo en atoms and su phonic and carboxyl groups.
  • v p i v V .5 A proeess'o colour ph t g aphy which comprises forming a reducible silver salt image in an emulsion layer of .a photographic element which contains a, compound oi the general formula:
  • hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X s para to the hydroxy group and is a member selected from the classiconsisting of the hydrogen and halogen atoms and sulphonic and carboxyl groups, and developing said image with an aromatic primary amino developing agent.
  • a process of colour photography which comprises forming a reducible silver salt image in an emulsion layer of a photographic element which contains a compound of the general formula:
  • hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the hydrogen and halogenatoms and sulphonic and carboxyl groups, and developing said image with an -N,N-dialky1-p-phenylene diamine.
  • i i 7 A process of colour photography which com prises forming a reducible silver salt image in an emulsionilayer of a photographic element which includes, adjacent thereto, a layer containing a compound of the general formula:
  • amino developing agent -(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethy
  • a process of colour photography which comprises torming a reducible silver salt image in an emulsion layer of a photographic element which includes, adjacent thereto, a layer containing a com ound of the general formula:
  • hydroxy group is in a. position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the hydrogen and halogen atoms and sulphonic and carboxyl groups, and developing said image with an N,N-dialkyl-p-phenylene diamine.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Patented May 11, 1948 CYANAGETYLAMINO PHENOL COLOR FORM- ERS FOR COLOR PHOTOGRAPHY John David Kendall and Douglas James-Fry, Ilford, England, assignors to Ilford Limited, Ilford, England, a British-companyv No Drawing. Application May 3, 1945, Serial No.
591,828. In Great Britain May 12, V
8 Claims.
1 p This invention relates to colour photography and particularly to dyestuff intermediates for use in colour photographic processes.
Processes of colour. photography are well known in which coloured images are produced by the development of reducible silver salt images by means of aromaticprimary amino develop-' ing agents in the presence of compounds, generally known as colour-formers" or colourcouplers, which couple with theoxidation products of such developers, formed during development, to form quinone-imine or azomethine dyes. The colour-couplers may be present in the developing solution employed, or may be included in a photographic emulsion layer which contains the reducible silver salt image, or in an adjacent layer or a layer separated from the said emulsion layer only by a thin Water-permeable layer. Thedeveloping agent may be, for example, p-phenylene diamine or its N.N.-dialkyl derivatives, e. g. N.N.-dimethyl and N.N.-diethyl p-ph'enylene diamines, or a homologue, e. g. 5-diethylamino-2- amino-toluene.
Large numbers of colour-couplers have been described in the extensive literature dealing with this type of colour photographic process. The requirements for a satisfactory colour-coupler, however, are rather strict. Thus it must be capable of ready incorporation into the developing bath or photographic layer'into which itis desired to include it, and where it is included ina photographic layer, neither it nor the dye derived from it must have any substantial tendency to diffuse from such layer, either into adjacent layers of the photographic element, or into processing baths. Moreover, it must be selected so that thecolourTof the dye obtained from it issuitable for the particular colour process with which it is intended to be used. 4
According to the present invention ja'process of colour photography comprises developing a reducible silver. salt image by means of an aro-v matic primary amino developing agent in the presence of a cyanaetylamino phenol of the general formula:
phonic, carboxyl, or halogen (or other atom or group readily removed during the dye-coupling reaction), or in the presence of a correspondin naphthol or higher homologous compound.
7 Such compoundsmay be prepared by reacting together an aminophenol (or naphthol or higher homologous compound) 'which is unsubstituted in' the para position tothe hydroxy group, or contains i a carboxyLsulphonic, halogen or other easily removable atom'or group in such position, with ethyl cyanacetate. Thus, for example, cyanacet-o-hydroxy-anilide may be prepared from o-amino-phenol and 'ethylcyanacetate in hot xylene solution in the presence of piperidine or other base. The'product separates on cooling, and after purification has a melting point of 178" 0. Similarly, using 2-amino-5-methyl phenol, the compound cyan'acet-o-h'ydroxy-p-toluidine, M.Pt. 189 C., is obtained. Both these compounds yield deep blue to blue-green dyes on colour-coupling development in accordance with thisinvention. Y
Other amino phenols and ,amino naphthols which may be similarly employed as initial reagents .are; for example, m-amino-phenol, 3- amino-e-naphthol, ,2-amino-5-ethoxy phenol, 2- amino-3-methyl 'phenol and 2-amino-5-chlor ph'enol. 1
Particular compounds which may be employed arez' 1-cyanacetylamino-2ehydroxy-l-ethoxy benzene 2-cyan'acetylamino l-hydroxy naphthalene I-cyanacetyIaminO-2-hydroxy-6-methyl benzene These compounds are made by the general process described above, using the appropriate reagents.
As will be clear from the foregoing discussion of the compounds, the benzene, naphthalene or other ring system present may'contain other substituent groups, e; g. hydrocarbon groups or alkoxy groups. 1 The colour-couplers of this invention maybe included in a developing solution containin an aromatic primary amino developing agent, or may be included in a silver halide emulsion layer, or in a water-permeable colloid layer coated next to a silver halide emulsion layer, or separated therefrom only by a thin water-permeable layer. Thus, for example, the colour-couplers of this invention may be used in any of the colour processes of U. S. Patents Nos. 2,350,380, 2,363,764 and 2,369,171 and British Patents Nos. 551,116, 551,117, 554,302 and 556,858.
The formation of coloured images by means of the colour-couplers of this invention may be applied to the development of a reducible silver salt image which is an original latent image formed in the emulsion layer by exposure to light, or which is an image obtained by the conversion of a silver image to areducible silver salt i a e by the usual ble hin techni ue;
Although this invention is primarily concerned with colour photographic processes in which the dye is formed by the coupling of the colourcouplers of the invention with the endatienprednets of an aromatic primary amino developing agent formed in situ during the deyeiopment, of a reducible silver salt image, ;th'e colours-couplers of the invention may also be employed in other colour photographic processes, ,e, g, .processesin which the dye is formed by direct coupling between the colour-coupler and a nitroso aniline, e. g. penitroso dialkyl aniline, or between the colour-coupler and a diazo compound. As an examp e f. t s latter time Qf.- processes 9191. 1:- up er m be P s nt in a layer so aim-nee e bl si e t ima e, s ch mage .1: oped w th ar mat c p imary i lino dev. opin age trermin an a omethi idyeimase .situ with t e dev lop dsi er ima e, the esidua o o ler c p d it .;.a diet-to compound ppl di ution, t the ph tos arms el ment and t e n l az meth ne .de image bleached out, eavi only he az .dyeuiinage n the layer.
What-We claim 7 V 1. A process of c lour photegraphy which coinprises developing a, redlleibie silver salt image in a photograph c elementby means of. an arsomatie p imary amine eerelep ng a enti the presence of a c mpound oi v-thesenerel formul where the hydroxy group in a position taken from the group consisting of ortho and meta positions to the cyanacetylaminogroup andwhere ;X. is para to the hydroxy group and, is a member se, lected from the class consisting of the hydrogen and halogen atoms and 'sulphonic and carboxyl groups. I r .l 2, A process of colour photography which comprises developing a reducible silver salt in a pho tographic element by means ore solution of an aromatic primary amino developing agent containing a compoundei t g neral o mu V NH.CO.CH2.CN
from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the, hydrogen and halogen atoms and-sulphonic ande r ox l g ups. 1
4. A photographic element for colour photography which comprises a support bearing at least one layer of a light-sensitive silver halide emulsign and, adjacent thereto, a layer containing a compound of the general formula:
NH.OO.CH2.CN
where the hydroxy group is in a position taken frorn the group consisting of ortho and meta positions to the cyanacetylamino group and where X para to the hydroxy group and is a member selected from the class consisting .of the ydrogen 'andhalo en atoms and su phonic and carboxyl groups. v p i v V .5 A proeess'o colour ph t g aphy which comprises forming a reducible silver salt image in an emulsion layer of .a photographic element which contains a, compound oi the general formula:
where the hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X s para to the hydroxy group and is a member selected from the classiconsisting of the hydrogen and halogen atoms and sulphonic and carboxyl groups, and developing said image with an aromatic primary amino developing agent.
6. A process of colour photography which comprises forming a reducible silver salt image in an emulsion layer of a photographic element which contains a compound of the general formula:
where the hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the hydrogen and halogenatoms and sulphonic and carboxyl groups, and developing said image with an -N,N-dialky1-p-phenylene diamine. i i 7. A process of colour photography which com prises forming a reducible silver salt image in an emulsionilayer of a photographic element which includes, adjacent thereto, a layer containing a compound of the general formula:
' ATNHD 0.0Hz.CN
where the hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a memberseleoted from the class consisting of the hydrogen and halogen atoms and sulphonic and carboxyl groups, and developing said image with an aromatic primary. amino developing agent,-
8. A process of colour photography which comprises torming a reducible silver salt image in an emulsion layer of a photographic element which includes, adjacent thereto, a layer containing a com ound of the general formula:
NH.CO.CH1.CN
where the hydroxy group is in a. position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the hydrogen and halogen atoms and sulphonic and carboxyl groups, and developing said image with an N,N-dialkyl-p-phenylene diamine.
JOHN DAVID KENDALL. DOUGLAS'JAMES FRY.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS
US591828A 1944-05-12 1945-05-03 Cyanacetylamino phenol color formers for color photography Expired - Lifetime US2441491A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2507180A (en) * 1947-02-08 1950-05-09 Eastman Kodak Co Cyano acetamino color couplers
US2525503A (en) * 1946-01-10 1950-10-10 Gen Aniline & Film Corp Production of phenazonium dyestuff images
US2536010A (en) * 1947-07-11 1950-12-26 Gen Aniline & Film Corp Preparation of azine dyestuff images
US2595768A (en) * 1948-09-07 1952-05-06 Ilford Ltd Photographic color correction
DE1041357B (en) * 1957-07-31 1958-10-16 Agfa Ag Process and multilayer material for the production of yellow dye images by color development
US3909190A (en) * 1972-08-21 1975-09-30 Henkel & Cie Gmbh Hair dyeing process and composition containing {60 -cyano-methanesulfonamido-nitrobenzene derivatives

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2108602A (en) * 1935-03-21 1938-02-15 Eastman Kodak Co Photographic color-forming compounds
US2133937A (en) * 1937-02-15 1938-10-18 Du Pont Film Mfg Corp Color photography
US2181944A (en) * 1936-11-26 1939-12-05 Agfa Ansco Corp Production of black-and-white photographic pictures
US2220908A (en) * 1938-04-04 1940-11-12 Ilford Ltd Production of colored photographic images by color development
US2269481A (en) * 1938-08-03 1942-01-13 Ilford Ltd Production of colored photographic images
US2303380A (en) * 1937-08-06 1942-12-01 American Mach & Foundry Sewing apparatus
US2328652A (en) * 1941-04-18 1943-09-07 Du Pont Process of color photography and composition thereof
US2350380A (en) * 1940-08-01 1944-06-06 Du Pont Photography
US2367531A (en) * 1942-06-12 1945-01-16 Eastman Kodak Co Acylaminophenol photographic couplers
US2369929A (en) * 1943-03-18 1945-02-20 Eastman Kodak Co Acylamino phenol couplers
US2380809A (en) * 1939-12-11 1945-07-31 Verkinderen Honore Color couplers for photographic color development

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2108602A (en) * 1935-03-21 1938-02-15 Eastman Kodak Co Photographic color-forming compounds
US2181944A (en) * 1936-11-26 1939-12-05 Agfa Ansco Corp Production of black-and-white photographic pictures
US2133937A (en) * 1937-02-15 1938-10-18 Du Pont Film Mfg Corp Color photography
US2303380A (en) * 1937-08-06 1942-12-01 American Mach & Foundry Sewing apparatus
US2220908A (en) * 1938-04-04 1940-11-12 Ilford Ltd Production of colored photographic images by color development
US2269481A (en) * 1938-08-03 1942-01-13 Ilford Ltd Production of colored photographic images
US2380809A (en) * 1939-12-11 1945-07-31 Verkinderen Honore Color couplers for photographic color development
US2350380A (en) * 1940-08-01 1944-06-06 Du Pont Photography
US2328652A (en) * 1941-04-18 1943-09-07 Du Pont Process of color photography and composition thereof
US2367531A (en) * 1942-06-12 1945-01-16 Eastman Kodak Co Acylaminophenol photographic couplers
US2369929A (en) * 1943-03-18 1945-02-20 Eastman Kodak Co Acylamino phenol couplers

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2525503A (en) * 1946-01-10 1950-10-10 Gen Aniline & Film Corp Production of phenazonium dyestuff images
US2507180A (en) * 1947-02-08 1950-05-09 Eastman Kodak Co Cyano acetamino color couplers
US2536010A (en) * 1947-07-11 1950-12-26 Gen Aniline & Film Corp Preparation of azine dyestuff images
US2595768A (en) * 1948-09-07 1952-05-06 Ilford Ltd Photographic color correction
DE1041357B (en) * 1957-07-31 1958-10-16 Agfa Ag Process and multilayer material for the production of yellow dye images by color development
US3909190A (en) * 1972-08-21 1975-09-30 Henkel & Cie Gmbh Hair dyeing process and composition containing {60 -cyano-methanesulfonamido-nitrobenzene derivatives

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