GB255900A - Manufacture of azo-dyestuffs - Google Patents
Manufacture of azo-dyestuffsInfo
- Publication number
- GB255900A GB255900A GB18622/26A GB1862226A GB255900A GB 255900 A GB255900 A GB 255900A GB 18622/26 A GB18622/26 A GB 18622/26A GB 1862226 A GB1862226 A GB 1862226A GB 255900 A GB255900 A GB 255900A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- anisol
- chlor
- toluidide
- naphthylamide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000004519 manufacturing process Methods 0.000 title 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 230000008878 coupling Effects 0.000 abstract 2
- 238000010168 coupling process Methods 0.000 abstract 2
- 238000005859 coupling reaction Methods 0.000 abstract 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- 229920000742 Cotton Polymers 0.000 abstract 1
- 230000002152 alkylating effect Effects 0.000 abstract 1
- 239000000987 azo dye Substances 0.000 abstract 1
- 150000008049 diazo compounds Chemical class 0.000 abstract 1
- 239000000835 fiber Substances 0.000 abstract 1
- 238000007689 inspection Methods 0.000 abstract 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 abstract 1
- 238000006467 substitution reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
255,900. I.G. Farbenindustrie Akt.- Ges., (Assignees of Farbwerke vorm. Meister, Lucius, & Br³ning). July 25, 1925, [Convention date]. Addition to 231,529. Monoazo dyes; lakes.-Azo dyes are produced in substance, on a substratum, or on the fibre by coupling with 2 : 3-oxynaphthoic arylides the diazo compounds derived from bases of the general formula where R1 is an alkyl, aralkyl or aryl group, R2 an aryl group, and R3 an alkyl or aralkyl group; the products give redder hues than those obtained from the dvestuffs described in the parent Specification. In examples, 4-benzenesulphomethy]- amino-2-amino-1-anisol is diazotized and coupled with 2 : 3-oxynaphthoic-5-chlor-2-toluidide to produce the dyestuff in substance, or cotton is prepared with the component and dyed by treating with the diazo solution; bright claret-red tints are obtained. Similar dyestuffs are obtained by using other bodies of the above general formula e.g. the 4-mono- or dichlor-benzenesulphomethylamino-2-aminoanisols as diazo components, or by coupling with other 2 : 3-oxynaphthoric arylides. Specification 248,766 is referred to. The Specification as open to inspection under Sect. 91 (3) (a), comprises also a table showing the shades obtained from the dyestuffs from the following components :-4-benzenesulphomethyl. amino-2-amino-1-anisol and 2 : 3-oxynaphthoic-otoluidide; 4-chlorbenzenesulphoamino-2-amino-1- anisol and the o-toluidide or a-naphthylamide; 4- naphthalene - #- sulphomethylamino-2-amino-1- anisol and the 5-chlor-2-toluidide, 4-chlor-2-anisidide, and a- and #-naphthylamide ; 4-naphthalene - asulphomethylammo-2 - amino-1- anisol and the 4-chlor-2-anisidide and #-naphthylamide; 4- toluene - sulphomethylamino - 2 - amino - 1 - anisol and the o-toluidide, 4-chlor-2-anisidide, and alpha- and #-naphthylamide; and 4-toluene-sulphobenzylamino-2-amino-1-anisol and the 5-chlor-2- toluidide and #-naphthylamide. This subjectmatter does not appear in the Specification as accepted. 2-Amino-4-arylsulpho-alkyl (or aralkyl) amino- I-alkyl (aralkyl, or aryl) oxybenzences are obtained by causing an arylsulphochloride or a substitution product thereof to act on a 4-amino-2-nitro-1-alkyl (arlkyl, or aryl) -oxybenzene, alkylating or benzylating the product and reducing.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE255900X | 1925-07-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB255900A true GB255900A (en) | 1927-10-06 |
Family
ID=5965825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB18622/26A Expired GB255900A (en) | 1925-07-25 | 1926-07-26 | Manufacture of azo-dyestuffs |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB255900A (en) |
-
1926
- 1926-07-26 GB GB18622/26A patent/GB255900A/en not_active Expired
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