US2268274A - Azo dyestuffs - Google Patents
Azo dyestuffs Download PDFInfo
- Publication number
- US2268274A US2268274A US330530A US33053040A US2268274A US 2268274 A US2268274 A US 2268274A US 330530 A US330530 A US 330530A US 33053040 A US33053040 A US 33053040A US 2268274 A US2268274 A US 2268274A
- Authority
- US
- United States
- Prior art keywords
- parts
- artificial silk
- formula
- dyes
- shades
- 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 - Lifetime
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- 239000000975 dye Substances 0.000 description 15
- 229920002955 Art silk Polymers 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 5
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 5
- 239000001632 sodium acetate Substances 0.000 description 5
- 229960004249 sodium acetate Drugs 0.000 description 5
- 235000017281 sodium acetate Nutrition 0.000 description 5
- 229960003010 sodium sulfate Drugs 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 150000008049 diazo compounds Chemical class 0.000 description 3
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- VXEKDUAEWNPZAS-UHFFFAOYSA-N 2-(3-methylanilino)ethane-1,1-diol Chemical compound CC1=CC=CC(NCC(O)O)=C1 VXEKDUAEWNPZAS-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 150000004992 toluidines Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Definitions
- This invention relates to am dyestuffs, more particularly to those of the general formula:
- aryl means a radicle of the benzene series
- X8 have the aforesaid signification with coupling components which contain no substituents causing solubility in water.
- the new dyestuffs are especially useful for dyeing and printing acetate artificial silk, and the dyeings and printings thus obtained exhibit good fastness properties, particularly a good fastness to light.
- the dyestuffs thus formed are distinguished on account of their essentially better tinctorial power by the valuable property of being capable when mixed with a dispersing agent of being fixed on acetate artificial silk from a neutral bath.
- the addition of soap to the dyeing bath can be dispensed with in such a case.
- OHrCHzOH CH3 ore-onion is isolated and mixed with a dispersing agent. It dyes acetate artificial silk from a bath which only contains sodium sulfate but no soap, bright orange shades of good fastness.
- Example 2 The diazo solution prepared from 24.5 parts of 4-aminophenylsulfoylacetdimethylamide is combined with a hydrochloric acid solution of 20 parts of dihydroxyethyl-meta-toluidine. After the addition of sodium acetate the formed dyestuff of the formula:
- Example 3 When combining the diazocompound of 24.5 parts of 4-aminophenylsulfoylacetdime-thylamide with a hydrochloric acid solution of 15.5 parts of diethylaniline and isolating the formed dyestuff after the addition of sodium acetate it may be mixed with a dispersing agent. It corre- CHzCHzOH HaC following examples are given, the parts being by sponds with the formula:
- diazo component the diazocompound of 30 parts 29 Example 4 ries
- R means the radical of a member of the class 2537 parts of 4 aminophenylsulfoylacethydrox consisting of aniline and toluidine derivatives beyethylamide are diazotized and the diazosolution mg Substltllted at the o en atoms by a memthus obtained is combined with a hydrochloric of the class co sist g o alkyl and hydroxyacid solution of 15.5 parts of diethylaniline.
- alkyl groups a t X Sta for member of After the addition of sodium acetate the formed the group consisting of hydrogen, alkyl and hydyestufi of the formula: droxyalkyl, which dyestuifs are especially useful 11001120112 CHa-CHs is isolated and mixed with a dispersing agent. for dyeing and printing acetate artificial silk It dyes from a sodiumsulfate containing bath acefast shades.
- the diazosolution prepared from 29.2 parts of 25 3-chloro-4-aminophenylsulfoylacethydroxyethyl- HO CHZOH E amide is combined with a hydrochloric acid solu- N-oo-Cm-s0l-O O tion of 16.5 parts of hydroXyethylmeth'yl-meta- HrCHa toluidine and the formed dyestufi is isolated after the addition of sodiumacetate and mixed with a no which dyestuff dyes from a sodiumsulfate condispersing agent.
- the dyestufi thus obtained taining bath acetate artificial silk strong reddish of the formula: orange shades of good fastness to water and dyes acetate artificial silk from a sodium sulfate washing even strongly twisted dyed good being containing bath bright scarlet shades of a good dyed thoroughly therewith.
- aryl means a radicle of the benzene se-
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Patented Dec. 30, 1941 UNITED STATES PATENT OFFICE AZO DYESTUFFS Werner Zerweck and Wilhelm Kunze, Frankforton-the-Main-Fechenheim, Germany, assignors to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application April 19, 1940, Serial No. 330,530. In Germany May 4, 1939 4 Claims.
This invention relates to am dyestuffs, more particularly to those of the general formula:
wherein aryl means a radicle of the benzene series, and the X8 have the aforesaid signification with coupling components which contain no substituents causing solubility in water.
The new dyestuffs are especially useful for dyeing and printing acetate artificial silk, and the dyeings and printings thus obtained exhibit good fastness properties, particularly a good fastness to light.
By selecting the components in such a manner that at least one free aliphatic hydroxyl group is present in the molecule either of the diazo or the coupling component, the dyestuffs thus formed are distinguished on account of their essentially better tinctorial power by the valuable property of being capable when mixed with a dispersing agent of being fixed on acetate artificial silk from a neutral bath. The addition of soap to the dyeing bath can be dispensed with in such a case. Thus even a compact tissue or a strongly twisted yarn is dyed thoroughly.
In order to further illustrate our invention the are diazotized in the usual manner. The clear diazo solution is then added to a hydrochloric acid solution of 20 parts of dihydroxyethyl-metatoluidine with the addition of sodium acetate. When the dyestufi formation is complete the dyestuff of the formula:
OHrCHzOH CH3 ore-onion is isolated and mixed with a dispersing agent. It dyes acetate artificial silk from a bath which only contains sodium sulfate but no soap, bright orange shades of good fastness.
Example 2 The diazo solution prepared from 24.5 parts of 4-aminophenylsulfoylacetdimethylamide is combined with a hydrochloric acid solution of 20 parts of dihydroxyethyl-meta-toluidine. After the addition of sodium acetate the formed dyestuff of the formula:
Example 3 When combining the diazocompound of 24.5 parts of 4-aminophenylsulfoylacetdime-thylamide with a hydrochloric acid solution of 15.5 parts of diethylaniline and isolating the formed dyestuff after the addition of sodium acetate it may be mixed with a dispersing agent. It corre- CHzCHzOH HaC following examples are given, the parts being by sponds with the formula:
HaC
weight and all temperatures in degrees centigrade.
Escample 1 and dyes acetate artificial silk from a soap containing bath orange shades of good fastness.
When starting from 3-aminophenylsulfoylacetdimethylamide the formed dyestuff dyes reddish 21.4 parts of 4-aminophenyl-sulfoylacetamide yellow shades.
. diazo component the diazocompound of 30 parts 29 Example 4 ries, R means the radical of a member of the class 2537 parts of 4 aminophenylsulfoylacethydrox consisting of aniline and toluidine derivatives beyethylamide are diazotized and the diazosolution mg Substltllted at the o en atoms by a memthus obtained is combined with a hydrochloric of the class co sist g o alkyl and hydroxyacid solution of 15.5 parts of diethylaniline. alkyl groups a t X Sta for member of After the addition of sodium acetate the formed the group consisting of hydrogen, alkyl and hydyestufi of the formula: droxyalkyl, which dyestuifs are especially useful 11001120112 CHa-CHs is isolated and mixed with a dispersing agent. for dyeing and printing acetate artificial silk It dyes from a sodiumsulfate containing bath acefast shades.
tate artificial silk strong reddish orange shades 2. The .azo dyestufi of the formula:
of good fastness to water and washing even HRC CH CH strongly twisted dyed good being dyed thorough- I 2 3 1y therewith. n-oo-om-smOnmQ-w A similar dyestuff is obtained when using as H CHZOHa which dyestufi dyes acetate artificial silk from a of 4-aminophenylsulfoylacetdihydroxyethylamsoap containing bath orange shades of good fastide.
Example 5 H955- 3. The azo dyestuff of the formula:
The diazosolution, prepared from 29.2 parts of 25 3-chloro-4-aminophenylsulfoylacethydroxyethyl- HO CHZOH E amide is combined with a hydrochloric acid solu- N-oo-Cm-s0l-O O tion of 16.5 parts of hydroXyethylmeth'yl-meta- HrCHa toluidine and the formed dyestufi is isolated after the addition of sodiumacetate and mixed with a no which dyestuff dyes from a sodiumsulfate condispersing agent. The dyestufi thus obtained taining bath acetate artificial silk strong reddish of the formula: orange shades of good fastness to water and dyes acetate artificial silk from a sodium sulfate washing even strongly twisted dyed good being containing bath bright scarlet shades of a good dyed thoroughly therewith.
fastness to water, washing and light. 40 4. The azo dyestufi of the formula:
Similar valuable dyestufis are obtainedwhen HOOHTCHz CHzCHzOH using as coupling component diethylaniline or as l I diazo component the diazocompound of 3-chlorolTI'COCHTSOZQNZN 4-amino-phenylsulfoylacetdihydroxyethylamide H 01 CH3 CH1 v or of 2 chloro 4 ammophenylsulfoylacethydroxy which dyestuif dyes acetate artificial silk from a gi g fi' sodium sulfate containing bath bright scarlet 1 Azo dystuffs of the general formula, shades of a good fastness to water, washing and light.
WERNER ZERWECK. NO Calkyl0;Sary1-N=NR WILHELM KUNZE. X:
wherein aryl means a radicle of the benzene se-
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2268274X | 1939-05-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2268274A true US2268274A (en) | 1941-12-30 |
Family
ID=7993100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US330530A Expired - Lifetime US2268274A (en) | 1939-05-04 | 1940-04-19 | Azo dyestuffs |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2268274A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3039863A (en) * | 1959-11-19 | 1962-06-19 | Stauffer Chemical Co | Aryl sulfonyl acetamides as herbicides |
-
1940
- 1940-04-19 US US330530A patent/US2268274A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3039863A (en) * | 1959-11-19 | 1962-06-19 | Stauffer Chemical Co | Aryl sulfonyl acetamides as herbicides |
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