GB905983A - Process for the production of 3-(ª--phenyl-ª--acetylethyl)-4-hydroxy-coumarin - Google Patents
Process for the production of 3-(ª--phenyl-ª--acetylethyl)-4-hydroxy-coumarinInfo
- Publication number
- GB905983A GB905983A GB3255459A GB3255459A GB905983A GB 905983 A GB905983 A GB 905983A GB 3255459 A GB3255459 A GB 3255459A GB 3255459 A GB3255459 A GB 3255459A GB 905983 A GB905983 A GB 905983A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenyl
- acetylethyl
- coumarin
- hydroxy
- production
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/42—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4
- C07D311/44—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4 with one hydrogen atom in position 3
- C07D311/46—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4 with one hydrogen atom in position 3 unsubstituted in the carbocyclic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
3 - (a - phenyl - b - acetyl - ethyl) - 4 - hydroxycoumarin is prepared by condensation of benzaldehyde with acetone in aqueous medium in the presence of a basic condensation catalyst, removal of excess acetone from the reaction product and then condensation of the residue (which contains benzylidene acetone) with 4-hydroxycoumarin in the presence of quinoline sulphate as catalyst. A detailed example is given.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR805669A FR1271976A (en) | 1959-09-21 | 1959-09-21 | Process for preparing 3-alpha-phenyl-beta-acetylethyl-4-hydroxycoumarin |
GB3255459A GB905983A (en) | 1959-09-24 | 1959-09-24 | Process for the production of 3-(ª--phenyl-ª--acetylethyl)-4-hydroxy-coumarin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3255459A GB905983A (en) | 1959-09-24 | 1959-09-24 | Process for the production of 3-(ª--phenyl-ª--acetylethyl)-4-hydroxy-coumarin |
Publications (1)
Publication Number | Publication Date |
---|---|
GB905983A true GB905983A (en) | 1962-09-19 |
Family
ID=10340422
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3255459A Expired GB905983A (en) | 1959-09-21 | 1959-09-24 | Process for the production of 3-(ª--phenyl-ª--acetylethyl)-4-hydroxy-coumarin |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB905983A (en) |
-
1959
- 1959-09-24 GB GB3255459A patent/GB905983A/en not_active Expired
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