GB420825A - New dyestuff intermediates - Google Patents
New dyestuff intermediatesInfo
- Publication number
- GB420825A GB420825A GB1640933A GB1640933A GB420825A GB 420825 A GB420825 A GB 420825A GB 1640933 A GB1640933 A GB 1640933A GB 1640933 A GB1640933 A GB 1640933A GB 420825 A GB420825 A GB 420825A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- aldehyde
- diazotized
- bisulphite
- amino
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Abstract
Azoanthranilic acid is manufactured by coupling a diazotized 5-amino-2-acylaminobenzoic acid with an aldehyde-bisulphite compound of anthranilic acid and removing the aldehyde-bisulphite and acyl groups by hydrolysis, or by coupling diazotized 3-amino-6-nitrobenzoic acid with an aldehyde-bisulphite compound of anthranilic acid, reducing the nitrogroup and removing the aldehyde bisulphite group by hydrolysis. The product is an p intermediate for the production of metalliferous azo dyes containing two atoms of metal. In examples: (1) 5-aminoacetylanthranilic acid is diazotized and coupled with the monosodium salt of o -sulphomethylanthranilic acid and the product is boiled with caustic soda lye; (2) 3-amino-6-nitrobenzoic acid is diazotized and coupled with the monosodium salt of o -sulphomethylanthranilic acid and the product is boiled with caustic soda lye and then warmed with sodium sulphide solution. Specification 141,643, [Class 2 (iii)], is referred to. 5-Aminoacetylanthranilic acid may be obtained by the reduction of 5-nitroacetylanthranilic acid which is obtainable by the nitration of acetylanthranilic acid or by the oxidation of 5-nitroacetyl-o-toluidine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1640933A GB420825A (en) | 1933-06-07 | 1933-06-07 | New dyestuff intermediates |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1640933A GB420825A (en) | 1933-06-07 | 1933-06-07 | New dyestuff intermediates |
Publications (1)
Publication Number | Publication Date |
---|---|
GB420825A true GB420825A (en) | 1934-12-07 |
Family
ID=10076795
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1640933A Expired GB420825A (en) | 1933-06-07 | 1933-06-07 | New dyestuff intermediates |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB420825A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5801890A (en) * | 1993-12-15 | 1998-09-01 | Fuji Photo Optical Co., Ltd. | Taking lens system |
-
1933
- 1933-06-07 GB GB1640933A patent/GB420825A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5801890A (en) * | 1993-12-15 | 1998-09-01 | Fuji Photo Optical Co., Ltd. | Taking lens system |
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