GB191108704A - Improvements in the Manufacture and Production Of Compounds and Colouring Matters of the Anthracene Series. - Google Patents
Improvements in the Manufacture and Production Of Compounds and Colouring Matters of the Anthracene Series.Info
- Publication number
- GB191108704A GB191108704A GB191108704DA GB191108704A GB 191108704 A GB191108704 A GB 191108704A GB 191108704D A GB191108704D A GB 191108704DA GB 191108704 A GB191108704 A GB 191108704A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diaminoanthraquinone
- dichlor
- heating
- benzoyl chloride
- product
- 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
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
8704. Johnson, J. Y., [Badische Anilin & Soda Fabrik]. April 7. Anthraquinonephenanthridones, which are dves or intermediate products for dyes, are obtained by condensation of o - benzoylaminohalogenanthraquinones or halogen derivatives thereof. Products are specified from the following parent materials:-1-benzoylamino-2-bromanthraquinone, 1:4-dibenzoyldiamino-2 : 3-dichloranthraquinone, 1 - chlor - 2 - benzoylaminoanthraquinone, 2 - benzoylamino - 3 - halogenanthraquinone, 1:5- dichlor - 2:6 - dibenzoyldiaminoanthraquinone, 1:3:5:7-tetrabrom-2:6- dibenzoyldiaminoanthraquinone, o-chlorbenzoyl- 2-amino-1-chloranthraquinone; the chlorine atom can be removed from the last-mentioned product by means of copper powder. Specification 20,338/10 is referred to. Benzoylaminohalogenanthraquinones. - 1:4- Dibenzoylamino - 2:3 - dichloranthraquinone is obtained by chlorinating 1:4-diaminoanthraquinone in an indifferent solvent, and heating the product with benzoyl chloride in nitrobenzene solution; 1:5-dichlor-2:6-dibenzoylaminoanthraquinone is obtained by boiling 1:5-dichlor-2:6- diaminoanthraquinone with benzoyl chloride; 1:3:5:7-tetrabrom-2:6-dibenzoylaminoanthraquinone is obtained by treating 2:6-diaminoanthraquinone with bromine in an indifferent solvent such as glacial. acetic acid, and heating the product with benzoyl chloride in nitrobenzene solution; o-chlorbenzoyl-2-amino-1- chloranthraquinone is obtained by heating ochlorbenzoyl chloride with 1 - chlor - 2 - aminoanthraquinone.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB191108704T | 1911-04-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB191108704A true GB191108704A (en) | 1911-12-30 |
Family
ID=32498532
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191108704D Expired GB191108704A (en) | 1911-04-07 | 1911-04-07 | Improvements in the Manufacture and Production Of Compounds and Colouring Matters of the Anthracene Series. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB191108704A (en) |
-
1911
- 1911-04-07 GB GB191108704D patent/GB191108704A/en not_active Expired
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