GB191020025A - Manufacture and Production of New Azodyestuffs. - Google Patents
Manufacture and Production of New Azodyestuffs.Info
- Publication number
- GB191020025A GB191020025A GB191020025DA GB191020025A GB 191020025 A GB191020025 A GB 191020025A GB 191020025D A GB191020025D A GB 191020025DA GB 191020025 A GB191020025 A GB 191020025A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- phenolalkylethers
- chlor
- methyl
- reducing
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/16—Trisazo dyes
- C09B31/20—Trisazo dyes from a coupling component"D" containing a directive hydroxyl group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
20,025. Newton, P. A., [Farbenfabriken vorm. F. Bayer & Co.]. Aug. 27. Trisazo dyes are obtained by combining the diazo compounds of 5-amino-4-chlor-2-acidylamino-1-phenolalkylethers or 5-amino-4-methyl- 2-acidylamino-1-phenolalkylethers with 1:6- or 1:7-naphthylamine sulphonic acid, or a mixture thereof, re-diazotizing, and combining with a second molecular proportion of one of these acids or a mixture thereof, diazotizing again, and combining with 1:3- or 2:7-naphthol sulphonic acid, and finally splitting off the acidyl groups by saponification. The products dye cotton blue shades and may be diazotized on the fibre and developed with #-naphthol etc. 5- Amino-4-chlor-2-oxalylamino-1-anisol, 5-amino-4- methyl-2-formylamino-1-anisol and the corresponding phenetols are specified as first components. 5-Amino-4-chlor-2-acidylamino-1-phenolalkylethers are obtained by acidylizing 5-nitro-4- chlor-2-amino-1-phenolalkylethers and reducing. The ethyl ether may be obtained by treating nitro-p-dichlorbenzene with ethyl alcohol and caustic soda, reducing the resulting 4-chlor-2- nitro-1-phenetol, acetylizing the amino body, nitrating the product, and then reducing. 5-Amino-4-methyl-2-acidylamino-1-phenolalkylethers are obtained by acidylizing 5-nitro-4- methyl-2-amino-1-phenolalkylethers and reducing ; the ethyl ether may be obtained by nitrating 2-acetylamino-4-methyl-1-phenetol, and reducing the product.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB191020025T | 1910-08-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB191020025A true GB191020025A (en) | 1911-08-10 |
Family
ID=32492401
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191020025D Expired GB191020025A (en) | 1910-08-27 | 1910-08-27 | Manufacture and Production of New Azodyestuffs. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB191020025A (en) |
-
1910
- 1910-08-27 GB GB191020025D patent/GB191020025A/en not_active Expired
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