GB317194A - Improvements in and relating to the manufacture of ketones - Google Patents
Improvements in and relating to the manufacture of ketonesInfo
- Publication number
- GB317194A GB317194A GB1967528A GB1967528A GB317194A GB 317194 A GB317194 A GB 317194A GB 1967528 A GB1967528 A GB 1967528A GB 1967528 A GB1967528 A GB 1967528A GB 317194 A GB317194 A GB 317194A
- Authority
- GB
- United Kingdom
- Prior art keywords
- guaiacol
- acyl
- chloride
- employed
- monoalkyl ethers
- 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
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/54—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of compounds containing doubly bound oxygen atoms, e.g. esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
317,194. Boot's Pure Drug Co., Ltd., and Marshall, J. July 6, 1928. Acyl- and alkyl-phenols. - Acyl derivatives of monoalkyl ethers of catechol are made by treating aliphatic esters of the said monoalkyl ethers with aluminium chloride, two molecular proportions of the latter being employed to one of ester. The esters may be formed during the reaction by adding a fatty acid chloride to the monoalkyl ether. The aeyl group takes up the para-position to the hydroxyl group. In examples, 4-propionylguaiacol is obtained from guaiacol propionate, 4 - butylguaiacol from guaiacol butyrate, and 4-caproylguaiacol from guaiacol and caproyl chloride, nitrobenzene being employed as a solvent. The acyl groups may be reduced to alkyl groups, for example, by the Clemmensen process with amalgamated zinc and hydrochloric acid. The products are of therapeutic value.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1967528A GB317194A (en) | 1928-07-06 | 1928-07-06 | Improvements in and relating to the manufacture of ketones |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1967528A GB317194A (en) | 1928-07-06 | 1928-07-06 | Improvements in and relating to the manufacture of ketones |
Publications (1)
Publication Number | Publication Date |
---|---|
GB317194A true GB317194A (en) | 1929-08-15 |
Family
ID=10133311
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1967528A Expired GB317194A (en) | 1928-07-06 | 1928-07-06 | Improvements in and relating to the manufacture of ketones |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB317194A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1988009321A1 (en) * | 1987-05-21 | 1988-12-01 | 3I Research Exploitation Limited | Substituted phenone |
-
1928
- 1928-07-06 GB GB1967528A patent/GB317194A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1988009321A1 (en) * | 1987-05-21 | 1988-12-01 | 3I Research Exploitation Limited | Substituted phenone |
US5037854A (en) * | 1987-05-21 | 1991-08-06 | 3I Research Exploitation Limited | Substituted phenone |
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