HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251406Generated: October 27, 2026
Methyl 3,3-diphenyloxirane-2-carboxylate → Methyl 2-hydroxy-3,3-diphenylbutyrate
https://huagongshe.com/reaction/251406
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 3,3-diphenyloxirane-2-carboxylate | HCID 10587027 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 2-hydroxy-3,3-diphenylbutyrate | HCID 11737309 | 16% |
Reaction Steps
1.5 g (5.9 mmol) of methyl 3,3-diphenyl-2,3-epoxypropionate dissolved in 10 ml of absolute ether were added dropwise to a cup-rate solution which had been prepared from 635 mg (7 mmol) of copper(I) cyanide dissolved in 10 ml of absolute ether and 8.14 ml (13 mmol) of a 1.6 normal methyllithium solution and had been cooled to −78° C. The solution was stirred at −78° C. for 1 h and then allowed to warm to room temperature. It was subsequently diluted with 100 ml of ether and 100 ml of water, and the ether phase was washed with dilute citric acid and with sodium bicarbonate solution and dried over magnesium sulfate. The crude product was purified by chromatography on silica gel with cyclohexane/ethyl acetate mixtures to result in 250 mg (16%) of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863445B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-6961d1c367824e28a6c271aaa7e7c812 |
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| Source note | uspto-grants-2011_01 |
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