GB809043A - New dyestuffs of the anthraquinone series - Google Patents
New dyestuffs of the anthraquinone seriesInfo
- Publication number
- GB809043A GB809043A GB2594156A GB2594156A GB809043A GB 809043 A GB809043 A GB 809043A GB 2594156 A GB2594156 A GB 2594156A GB 2594156 A GB2594156 A GB 2594156A GB 809043 A GB809043 A GB 809043A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alcohol
- aminoanthraquinone
- nitro
- chloride
- acid
- 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
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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/22—Dyes with unsubstituted amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
5 - Nitro - 1 - aminoanthraquinone - 2 - carbonyl chloride is made by reacting 5-nitro-1-aminoanthraquinone-2-carboxylic acid with thionyl chloride in nitrobenzene at 85 DEG C., cooling the mixture and filtering off the product. Specification 267,164, [Class 2 (3)], is referred to.ALSO:The invention comprises red dyes of the formula <FORM:0809043/IV (c)/1> where n is 1, 2 or 3 and R is hydrogen or alkyl, and a process for making them either by heating 5-nitro-1-aminoanthraquinone-2-carboxylic acid with an alcohol of the formula H(OCH2CH2)nOR or by treating the corresponding acid chloride with such an alcohol. Excess alcohol may be present, and sulphuric acid or hydrogen chloride may be used to catalyse the reaction between the acid and alcohol. Alcohols which may be used are 1 : 2-di-(b -hydroxyethoxy)-ethane, B : B1 - dihydroxydiethylether, diethyleneglycol monoethylether, ethylene glycol, ethyleneglycol monobutylether and diethyleneglycol monomethyl ether. Examples are given. The dyestuffs may be used for dyeing acetate rayon and polyethylene terephthalate, and may be dispersed by milling with sodium methylene bis-(naphthalene-2-sulphonate) to form an aqueous paste, which may be dried, if desired, to form a re-dispersible powder. Specification 267,164, [Class 2 (3)], is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2594156A GB809043A (en) | 1956-08-24 | 1956-08-24 | New dyestuffs of the anthraquinone series |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2594156A GB809043A (en) | 1956-08-24 | 1956-08-24 | New dyestuffs of the anthraquinone series |
Publications (1)
Publication Number | Publication Date |
---|---|
GB809043A true GB809043A (en) | 1959-02-18 |
Family
ID=10235805
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2594156A Expired GB809043A (en) | 1956-08-24 | 1956-08-24 | New dyestuffs of the anthraquinone series |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB809043A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2417527A1 (en) * | 1978-02-17 | 1979-09-14 | Bayer Ag | NEW ANTHRAQUINONIC DYES THAT DO NOT CONTAIN NITRO GROUPS AND SULPHONIC ACID GROUPS |
-
1956
- 1956-08-24 GB GB2594156A patent/GB809043A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2417527A1 (en) * | 1978-02-17 | 1979-09-14 | Bayer Ag | NEW ANTHRAQUINONIC DYES THAT DO NOT CONTAIN NITRO GROUPS AND SULPHONIC ACID GROUPS |
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