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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120141Generated: October 30, 2026

Hydrochloric Acid → (2S,3S)-3-[[1-(S)-[alpha-(R)-hydroxybenzyl]-3-methylbutyl]-carbamoyl]oxirane-2-carboxylic acid

https://huagongshe.com/reaction/2120141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantPotassium hydroxide ethanolHCID 21946426—
Reactant[1-(S)-[alpha-(R)-hydroxybenzyl]-3-methylbutyl carbamoyl]oxirane-2-carboxylateHCID 86585457—
Product(2S,3S)-3-[[1-(S)-[alpha-(R)-hydroxybenzyl]-3-methylbutyl]-carbamoyl]oxirane-2-carboxylic acidHCID 12051469—

Reaction Steps

To a solution of ethyl (2S,3S)-3-[[1-(S)-[α-(R)-hydroxybenzyl]-3-methylbutyl carbamoyl]oxirane-2-carboxylate (558 mg, 1.66 mmol.) in ethanol (4 mL) was dropwise added 0.5N potassium hydroxide/ethanol solution (4.0 mL, 2.0 mmol.) under chilling with ice The mixture was stirred for 4 hours at room temperature, and made acidic to reach pH 1-2 by addition of water (40 m) and 2N hydrochloric acid (approx. 2 mL). The acidic mixture was extracted with three portions of ethyl acetate. The three extracts were combined and washed successively with water and an aqueous saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to give the titled compound as a white amorphous product (490 mg, yield 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689785B2
Source datasetuspto-grants-2004_02
ORD IDord-148a037393904f8baac01f5e6bb49111
Source noteuspto-grants-2004_02