GB300114A - Manufacture of indigoid vat dyestuffs - Google Patents
Manufacture of indigoid vat dyestuffsInfo
- Publication number
- GB300114A GB300114A GB7241/28A GB724128A GB300114A GB 300114 A GB300114 A GB 300114A GB 7241/28 A GB7241/28 A GB 7241/28A GB 724128 A GB724128 A GB 724128A GB 300114 A GB300114 A GB 300114A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chlor
- methyl
- hydroxy
- chloride
- methylisatin
- 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
- C09B7/06—Indone-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Abstract
300,114. I. G. Farbenindustrie Akt.- Ges. Nov. 5, 1927, [Convention, date]. Addition to 282,805. Thioindigo dyes,-A, derivative of 3-hydroxy-1- thionaphthalene substituted in the nucleus is condensed with 7-methylisatin-a-chloride substituted by halogen or methyl in the 5-position or by halogen or methyl or halogen and methyl in the 4-and 5-positions. According to examples the following pairs of components are condensed : 5-chlor-7-methyl-or 4-methyl-6-chlor-3-hydroxy-1- thionaphthene and 4: 7 -dimethyl-5-chlorisatina-chloride: 5 : 6 : :7-trichlor-3-hydroxy-1-thionaphthene; and 4 : 7-dimethyl-5-chlorisatin-a-chloride 4-methyl - 5 : 7-dichlor-3-hydroxy-1-thionaphthene and 5-chlor-7-methyl-or 5: 7-dimethylisatin-achloride; 4 : 7-dimethyl-5-chlor-3-hydroxy-i-thionaphtheno and 5-chlor-7 -methylisatin-a-chloride. Specification 283,118 is referred to. Isatin, derivatives.-4-Chlor-2-toluidine, 5-chlor- 2-toluidine and p-xylidine are converted into the a-toluidides and a-xylidide of the corresponding isatins by the process of German Specification 277,396, by forming the hydrocyanocarbodiarylimides and effecting ring closure. The achlortoluidides and the a-xylidide may be saponified to give 4-chlor- and 5-chlor-7-methylisatin and 4 : 7-dimethylisatin respectively. The latter may be chlorinated in acetic acid solution to give 4 : 7-dimethvl-5-chlorisatin.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE300114X | 1927-11-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB300114A true GB300114A (en) | 1929-03-07 |
Family
ID=6092019
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7241/28A Expired GB300114A (en) | 1927-11-05 | 1928-03-08 | Manufacture of indigoid vat dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB300114A (en) |
-
1928
- 1928-03-08 GB GB7241/28A patent/GB300114A/en not_active Expired
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