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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456610Generated: October 31, 2026

Benzhydrylamine → Ethyl (2S,3S)-3-diphenylmethylcarbamoyloxirane-2-carboxylate

https://huagongshe.com/reaction/1456610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrylamineHCID 7036—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant(2S,3S)-3-(ethoxycarbonyl)oxirane-2-carboxylic acidHCID 11030109—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductEthyl (2S,3S)-3-diphenylmethylcarbamoyloxirane-2-carboxylateHCID 57291692—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of (2S,3S)-3-ethoxycarbonyloxirane-2-carboxylic acid (8.01 g, 50.0 mmol.) in ethyl acetate (120 mL) was added N-hydroxysuccinimide (5.76 g, 50.0 mmol.) and then added N,N'-dicyclohexylcarbodiimide (5.75 g, 50.0 mmol) under chilling with ice. The resulting mixture was stirred at 5° C. for one hour, and to the mixture was a solution of aminodiphenylmethane (9.17 g, 50.0 mmol.) in ethyl acetate (30 mL). The mixture was stirred at 5° C. for one hour and then at room temperature for one hour. The resulting N,N'-dicyclohexylurea (DC-Urea) was removed by filtration, and the filtrate was washed successively with 1N hydrochloric acid, an aqueous sodium hydrogen carbonate saturated solution, and an aqueous sodium chloride saturated solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was recrystalized from ethyl acetate--n-hexane, to give the desired compound as a white crystalline product (1.25 g, yield: 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843992
Source datasetuspto-grants-1998_12
ORD IDord-320293505c3847a19e7a6b4387c7b2cf
Source noteuspto-grants-1998_12