GB191212162A - Manufacture and Production of Carboxydiarylhydrols. - Google Patents
Manufacture and Production of Carboxydiarylhydrols.Info
- Publication number
- GB191212162A GB191212162A GB191212162DA GB191212162A GB 191212162 A GB191212162 A GB 191212162A GB 191212162D A GB191212162D A GB 191212162DA GB 191212162 A GB191212162 A GB 191212162A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- carboxylic acid
- xylenol
- cresotinic
- carboxydiarylhydrols
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
12,162. Newton, P. A., [Farbenfabriken vorm. F. Bayer & Co.]. May 22. Carboxydiarylhydrols are obtained by condensing one molecule of a substituted benzaldehyde with one molecule of an aromatic o-oxvcarboxylic acid. According to an example, pdiethylaminobenzaldehyde and s-xylenol-o-carboxylic acid are condensed in sulphuric acid solution; products are also described from the following pairs of substances : -o-chlorbenzaldehyde and s-xylenol-o-carboxylic acid, 2:6-dichlorbenzaldehyde and m-cresotinic acid. 2:6- dichlor-3-oxybenzaldehyde and m-cresotinic acid, 2:6-dichlor-3-methoxybenzaldehyde and sxylenol-ocarboxylic acid, o-sulphobenzaldehyde and m-cresotinic acid or s-xylenol-o-carboxylic acid, 2-chlor-o-sulphobenzaldehyde and s-xylenolo-carboxylic acid, 2:5-disulphobenzadehyde and s-xylenol-o-carboxylic acid, p-diethylaminobenzaldehyde and 2-naphthol-3-carboxylic acid, ochlor-p-dimethylaminobenzaldehyde and mcresotinic acid or s-xylenol-o-carboxylic acid, o-chlor-p-diethylaminobenzaldehyde and m- or p-cresotinic acid, s-xylenol-o-carboxylic acid, or 1-naphthol-2-carboxylic acid; polychlorbenzaldehydes, 3-methyl-2-oxy-4-chlorbenzoic acid, and sulphonic acids of the oxycarboxylic acids are also mentioned as parent materials. Triarylmethane dyes are obtained by condensing the above-described carboxydiarylhydrols with aromatic o-oxycarboxylic acids and oxidizing the leuco bodies so produced; products are described from o-cresotinic acid and the specific hydrols mentioned above; these dye wool blue to violet shades with chrome mordants.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB191212162T | 1912-05-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB191212162A true GB191212162A (en) | 1913-01-16 |
Family
ID=32572296
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191212162D Expired GB191212162A (en) | 1912-05-22 | 1912-05-22 | Manufacture and Production of Carboxydiarylhydrols. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB191212162A (en) |
-
1912
- 1912-05-22 GB GB191212162D patent/GB191212162A/en not_active Expired
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