GB1327011A - Production of flavanthrenes - Google Patents
Production of flavanthrenesInfo
- Publication number
- GB1327011A GB1327011A GB57371A GB57371A GB1327011A GB 1327011 A GB1327011 A GB 1327011A GB 57371 A GB57371 A GB 57371A GB 57371 A GB57371 A GB 57371A GB 1327011 A GB1327011 A GB 1327011A
- Authority
- GB
- United Kingdom
- Prior art keywords
- solution
- flavanthrene
- dianthraquinonyl
- jan
- formula
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/20—Flavanthrones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1327011 Flavanthrene BADISCHE ANILIN - & SODA-FABRIK AG 6 Jan 1971 [7 Jan 1970] 573/71 Heading C4P Flavanthrenes having the formula wherein X is a hydrogen or halogen atom, are obtained by subjecting a 2,2<SP>1</SP>-diacylamino-1,1<SP>1</SP>- dianthraquinonyl of formula where R is an alkyl group having 1-6 carbon atoms or an unsubstituted aryl group, to intramolecular condensation under the action of H 2 SO 4 having a concentration of 80-100% by wt. The treatment is advantageously carried out at 20-70‹ C., the dianthraquinonyl derivative preferably being added to 93-99% sulphuric acid to give a pink solution which is stirred until an intense red solution is obtained which vats with a blue colour. The solution is then poured into water to precipitate the flavanthrene. The products are yellow vat dyes.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19702000510 DE2000510C3 (en) | 1970-01-07 | 1970-01-07 | Process for the production of flavanthrenes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1327011A true GB1327011A (en) | 1973-08-15 |
Family
ID=5759145
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB57371A Expired GB1327011A (en) | 1970-01-07 | 1971-01-06 | Production of flavanthrenes |
Country Status (4)
Country | Link |
---|---|
CH (1) | CH550228A (en) |
DE (1) | DE2000510C3 (en) |
FR (1) | FR2075973B3 (en) |
GB (1) | GB1327011A (en) |
-
1970
- 1970-01-07 DE DE19702000510 patent/DE2000510C3/en not_active Expired
- 1970-12-09 CH CH1819170A patent/CH550228A/en not_active IP Right Cessation
-
1971
- 1971-01-06 GB GB57371A patent/GB1327011A/en not_active Expired
- 1971-01-07 FR FR7100307A patent/FR2075973B3/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR2075973B3 (en) | 1973-10-19 |
DE2000510B2 (en) | 1974-09-19 |
DE2000510A1 (en) | 1971-07-15 |
DE2000510C3 (en) | 1975-05-15 |
CH550228A (en) | 1974-06-14 |
FR2075973A7 (en) | 1971-10-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PE20 | Patent expired after termination of 20 years |