GB263879A - Manufacture of dyestuffs of the triarylmethane series - Google Patents
Manufacture of dyestuffs of the triarylmethane seriesInfo
- Publication number
- GB263879A GB263879A GB127/27A GB12727A GB263879A GB 263879 A GB263879 A GB 263879A GB 127/27 A GB127/27 A GB 127/27A GB 12727 A GB12727 A GB 12727A GB 263879 A GB263879 A GB 263879A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cresotinic
- mol
- mols
- dyestuffs
- 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
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/10—Amino derivatives of triarylmethanes
- C09B11/22—Amino derivatives of triarylmethanes containing OH groups bound to an aryl nucleus and their ethers and esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lasers (AREA)
Abstract
263,879. I. G. Farbenindustrie Akt.- Ges. Jan. 2, 1926, [Convention date]. Triarylmethane dyes.-Water soluble chrome dyestuffs of the triarylmethane series are produced by treating substituted aryldi-0-cresotinicacid carbinol with a normal sulphite. In examples. p-(4-tolyamino)-phenyldi-o-cresotinic acidcarbinol and p-(6-chlor-2-tolylamino)-phenyldi-o-cresotinic acidcarbinol are heated with crystallized sodium sulphite in the presence of water and, if necessary filtered. On acidifying the solution the original carbinol is reprecipitated. In other examples the dyestuff made from 2 mols. of o. cresotinic acid, 1 mol. p-chlorbenzaldehyde and J. mol. of 1-chlor-2-naphthylamine and that from 2 mols. o-cresotinic acid, 1 mol. of p-chlorbenzaldehyde and 1 mol. of pyridine are heated with crystallized sodium sulphite in the presence of water and in further examples the dyestuffs made by coupling 1 molecular proportion each of o, o<1>- dichlorbenzaldehyde, o, o<1>-dichlor-m-hydroxybenzaldehyde, 2:4: 6-tribrom-3-hydroxybenzaldehyde and the hydroxynaphthaldehyde disulphonic acid obtainable according to example 2 of Specification 19408/97 with 2 mols. of o-cresotinic acid are treated with sodium sulphite in the same way. Specifications 15204/07, 12130/10, and 237,096 also are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE263879X | 1926-01-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB263879A true GB263879A (en) | 1927-07-28 |
Family
ID=5986585
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB127/27A Expired GB263879A (en) | 1926-01-02 | 1926-01-03 | Manufacture of dyestuffs of the triarylmethane series |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB263879A (en) |
-
1926
- 1926-01-03 GB GB127/27A patent/GB263879A/en not_active Expired
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