GB431708A - Process for the manufacture of acid safranine dyestuffs - Google Patents
Process for the manufacture of acid safranine dyestuffsInfo
- Publication number
- GB431708A GB431708A GB1500/34A GB150034A GB431708A GB 431708 A GB431708 A GB 431708A GB 1500/34 A GB1500/34 A GB 1500/34A GB 150034 A GB150034 A GB 150034A GB 431708 A GB431708 A GB 431708A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- diethylisorosinduline
- dimethyl
- sulphonic
- diaminobenzene
- 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
- C09B17/00—Azine dyes
- C09B17/04—Azine dyes of the naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Safranine dyestuffs which dye wool greenish blue shades are obtained by condensing isorosinduline sulphonic acids of the formula <FORM:0431708/IV/1> in which R1 and R2 are alkyl, aralkyl or aryl, with aromatic 1 : 4 diamines which are not substituted in both amino groups and contain in the 2-position an alkyl group or in the 2 and 6 positions neutral substituents such as alkyl, oxyalkyl or halogen. Sulphonic groups may be introduced into the safranines by sulphonation or sulphonated 1 : 4-diamines may be used, and the products may be treated with alkylating or acylating agents. In examples: (1) the isorosindulinetrisulphonic acid obtainable from 4<1>-acetylamino-2<1>-sulphophenyl-b -naphthylamine and 4-aminodiethylaniline-3-sulphonic acid or 11 : 13-dichlor diethylisorosinduline-1 : 6-disulphonic acid is heated with 2 : 6-dimethyl-1 : 4-diaminobenzene to give the corresponding safranine; (2) diethylisorosinduline - 11 - methyl - 1 : 6 - disulphonic acid is condensed with toluylenediamine or 2 : 6-dichlor-1 : 4-phenylenediamine and then treated with oleum; (3) 2 : 6-dimethyl-1 : 4-diaminobenzene-3-sodium suphonate is condensed with 11 - methyl - diethylisorosinduline - 1 : 6 - disulphonic acid or 11-methyl-14-chlor-diethylisorosinduline-1 : 6-disulphonic acid. 2 : 6 - Dimethyl - 1 : 4 - diaminobenzene - 3 - sulphonic acid may be prepared by coupling a diazo compound with 1-amino-2 : 6-dimethylbenzene, reducing the azo compound to 2 : 6-dimethyl-1 : 4-phenylenediamine and sulphonating the latter.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE431708X | 1933-01-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB431708A true GB431708A (en) | 1935-07-15 |
Family
ID=6488683
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1500/34A Expired GB431708A (en) | 1933-01-14 | 1934-01-15 | Process for the manufacture of acid safranine dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB431708A (en) |
-
1934
- 1934-01-15 GB GB1500/34A patent/GB431708A/en not_active Expired
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