GB222094A - Manufacture of vat dyestuffs containing sulphur - Google Patents
Manufacture of vat dyestuffs containing sulphurInfo
- Publication number
- GB222094A GB222094A GB19818/24A GB1981824A GB222094A GB 222094 A GB222094 A GB 222094A GB 19818/24 A GB19818/24 A GB 19818/24A GB 1981824 A GB1981824 A GB 1981824A GB 222094 A GB222094 A GB 222094A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxythionaphthene
- methyl
- anil
- ethoxy
- nucleal
- 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
- C09B7/00—Indigoid dyes
- C09B7/10—Bis-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Thioindigoid dyes are prepared by heating a 2-anil/mm of a 2 : 3-diketodihydro-6-alkyloxy-thionaphthene or a nucleal substitution product thereof with a nucleal substitution product of 3-oxythionaphthene, or by heating a 3-oxy-6-alkyl-oxythionaphthene or a nucleal substitution product thereof with a nucleal substitution product of 2 : 3-diketodihydrothionaphthene-2-anil; a solvent may be present. The products dye cotton in red shades which resemble those of alizarin and which may be influenced towards blue or towards yellow by introduction of further substituents. According to examples the following pairs of components are used:-6-ethoxy-3-oxythionaphthene and 4-methyl-6-chloro- or 6-bromo-2 : 3-dihydro-3-keto-2 (p-dimethylamino)- anil; 6-ethoxy-2 : 3-dihydro-3-ketothionaphthene-2- (p-dimethylamino)-anil and 4-methyl-6-bromo-3-oxythionaphthene or 4-methyl-5 : 6-dichloro-3-oxythionaphthene; 6-methoxy-3-oxythionaphthene and 4-methyl-6-bromo-2 : 3-dihydro-3-ketothionaphthene-2(p-dimethylamino)-anil. 4-Methyl-6-chloro-, 4-methyl-6-bromo-, and 6-ethoxy - 2 : 3-dihydro-3-ketothionaphthene - 2 - (p-methylamino) anils are obtained by action of nitrosodimethylaniline upon the corresponding 3-oxythionaphthenes in alkaline solution. Oxythionaphthenes. - 5-Brom-6-ethoxy-3-oxythionaphthene is obtained from 4-ethoxy-2-thioglycol-1-carboxylic acid by bromination and ring closure. 4-Methyl-5 : 6-dichloro-3-oxythionaphthene is obtained from 1-methyl-2-amino-3-chlorobenzene-5-sulphonic acid by exchanging the amino group for chlorine, converting the sulphonic acid into the thioglycollic acid and effecting ring closure in known manner. Specifications 28240/06 and 10541/07 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE222094X | 1923-09-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB222094A true GB222094A (en) | 1925-08-27 |
Family
ID=5843578
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19818/24A Expired GB222094A (en) | 1923-09-17 | 1924-08-21 | Manufacture of vat dyestuffs containing sulphur |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB222094A (en) |
-
1924
- 1924-08-21 GB GB19818/24A patent/GB222094A/en not_active Expired
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