Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 4-(m-benzoyl-phenyl)-3-hydroxybutyrate | HCID 21495623 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21495680 | HCID 21495680 | 96% |
Reaction Steps
2.7 ml of water and 1.4 ml of 12.5N potassium hydroxide were added to a solution of 2.7 g of ethyl 4-(m-benzoylphenyl)-3-hydroxy-butyrate in 27 ml of ethanol and the mixture was refluxed for 11/2 hours and then evaporated to dryness. The residue as taken up in 27 ml of water and the solution was treated with activated carbon, filtered and acidified to a pH of 1 by adding 10 ml of 2N hydrochloric acid with stirring at 10° C. The mixture was extracted with methylene chloride and the organic phase was washed with water, dried over sodium sulfate, treated with activated carbon, filtered and evaporated to dryness to obtain 2.36 g of 4-(m-benzoyl-phenyl)-3-hydroxy-butyric acid in the form of a colorless amorphous solid soluble in chloroform and insoluble in water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03995056 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-41663c2b83d8422d9a042b2cae8a8918 |
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| Source note | uspto-grants-1976_11 |
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