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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491736Generated: October 31, 2026

Benzoic Acid → [(1S)-1-[(2R)-2-(2,4-difluorophenyl)-2-oxiranyl]ethyl]benzoate

https://huagongshe.com/reaction/1491736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(1R)-1-[(2R)-2-(2,4-difluorophenyl)-2-oxiranyl]ethanolHCID 10536015—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product[(1S)-1-[(2R)-2-(2,4-difluorophenyl)-2-oxiranyl]ethyl]benzoateHCID 1070960578.5%

Reaction Steps

To a solution of 16.1 g of (1R)-1-[(2R)-2-(2,4-difluorophenyl)- 2-oxiranyl]ethanol in 320 ml of tetrahydrofuran were added, with ice cooling, 63.3 g of triphenylphosphine, 29.5 g of benzoic acid and 42.0 g of diethyl azodicarboxylate and the mixture was stirred in an argon atmosphere at room temperature for 6 hours. To the reaction solution were added 800 ml of ethyl acetate and 500 ml of water to fractionate and the aqueous layer was extracted with 200 ml of ethyl acetate. The organic layers were combined, washed with water and saturated aqueous solution of sodium chloride, dried over magnesium sulfate and concentrated. The residue was purified by silica gel chromatography (eluate; hexane:ethyl acetate=15:1 to 7:1) to give 19.2 g of [(1S)-1-[(2R)-2-(2,4-difluorophenyl)-2-oxiranyl]ethyl]benzoate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371101
Source datasetuspto-grants-1994_12
ORD IDord-cab7a8565d3f4059ad5e6c58f6b5824c
Source noteuspto-grants-1994_12