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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166210Generated: November 2, 2026

Ethyl benzoylformate → (-)-Ethyl mandelate

https://huagongshe.com/reaction/2166210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl benzoylformateHCID 15349—
ReactantL-Tartaric acidHCID 444305—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product(-)-Ethyl mandelateHCID 6951556—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a dispersion of 0.43 g (11.3 mmol) of sodium borohydride in THF (35 ml), there was added 1.70 g (11.3 mmol) of L-(+)-tartaric acid, and the mixture was heated under reflux for four hours in an oil bath at 70° C. with stirring. The resulting mixture was cooled in a cryostat at -20° C., a solution of 0.5 g (2.8 mmol) of ethyl phenylglyoxylate in THF (5 ml) was added dropwise over a period of ten minutes, and stirring was continued for 19 hours. The reaction mixture was treated in the same manner as in Example 6, giving 0.44 of ethyl (R)-(-)-2-hydroxy-2-phenylacetate, having a specific rotation [α]D16 of -109° (cl. 00, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943652
Source datasetuspto-grants-1990_07
ORD IDord-23d7742559c24a7d8cf6c67f17defabd
Source noteuspto-grants-1990_07