GB361338A - Improvements in the manufacture and production of anthraquinone derivatives - Google Patents
Improvements in the manufacture and production of anthraquinone derivativesInfo
- Publication number
- GB361338A GB361338A GB1863130A GB1863130A GB361338A GB 361338 A GB361338 A GB 361338A GB 1863130 A GB1863130 A GB 1863130A GB 1863130 A GB1863130 A GB 1863130A GB 361338 A GB361338 A GB 361338A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diamino
- give
- treated
- solution
- methanol
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C50/00—Quinones
- C07C50/26—Quinones containing groups having oxygen atoms singly bound to carbon atoms
- C07C50/34—Quinones containing groups having oxygen atoms singly bound to carbon atoms the quinoid structure being part of a condensed ring system having three rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Alkyoxyanthraquinones are prepared by treating aryloxyanthraquinones with solutions of alkali metals or alkali metal hydroxides in monohydric alcohols. In examples (1) 1-phenoxyanthraquinone is treated with a solution of potassium hydroxide in methanol, ethanol or butanol to give 1-methoxyanthraquinone or the corresponding ethoxy or n-butyloxy derivative; (2) 1 : 4-diamino-2-phenoxy-anthraquinone is treated with a solution of potassium hydroxide in methanol, ethanol or n-butyl alcohol to give 1 : 4-diamino-2-methoxyanthraquinone or the corresponding ethoxy or n-butyloxy derivative; (4) 1 : 4 - diamino - 2 : 3 - diphenoxyanthraquinone is treated with a solution of potassium hydroxide in methanol, ethanol or butanol to give 1 : 4-diamino-2 : 3-dimethoxyanthraquinone or the corresponding diethoxy or dibutoxy derivatives; (5) 1-phenoxyanthraquinone is treated with a solution of potassium in methyl alcohol to give 1-methoxy-anthraquinone.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1863130A GB361338A (en) | 1930-06-18 | 1930-06-18 | Improvements in the manufacture and production of anthraquinone derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1863130A GB361338A (en) | 1930-06-18 | 1930-06-18 | Improvements in the manufacture and production of anthraquinone derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB361338A true GB361338A (en) | 1931-11-18 |
Family
ID=10115769
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1863130A Expired GB361338A (en) | 1930-06-18 | 1930-06-18 | Improvements in the manufacture and production of anthraquinone derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB361338A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2992240A (en) * | 1957-10-04 | 1961-07-11 | Ici Ltd | New dyestuffs |
CN113880698A (en) * | 2021-11-03 | 2022-01-04 | 济南周行医药科技有限公司 | Preparation method of 9, 10-dibutoxyanthracene |
-
1930
- 1930-06-18 GB GB1863130A patent/GB361338A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2992240A (en) * | 1957-10-04 | 1961-07-11 | Ici Ltd | New dyestuffs |
CN113880698A (en) * | 2021-11-03 | 2022-01-04 | 济南周行医药科技有限公司 | Preparation method of 9, 10-dibutoxyanthracene |
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