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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120144Generated: October 31, 2026

Acetic Anhydride → Ethyl (2S,3S)-3-[[1(S)-[alpha-(R)-acetoxybenzyl]-3-methyl-butyl]carbamoyl]oxirane-2-carboxylate

https://huagongshe.com/reaction/2120144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl (2S,3S)-3-[[1-(S)-[alpha-(R)-hydroxybenzyl]-3-methyl-butyl]carbamoyl]oxirane-2-carboxylateHCID 12051467—
SolventPyridineHCID 1049—
ProductEthyl (2S,3S)-3-[[1(S)-[alpha-(R)-acetoxybenzyl]-3-methyl-butyl]carbamoyl]oxirane-2-carboxylateHCID 12051480—

Reaction Steps

In pyridine (0.6 mL) was dissolved ethyl (2S,3S)-3-[[1-(S)-[α-(R)-hydroxybenzyl]-3-methylbutyl]carbamoyl]-oxirane-2-carboxylate (300 mg, 0.894 mmol.). To the resulting solution was added acetic anhydride (0.085 ML, 0.901 mml.) under chilling with ice. The mixture was stirred for 18 hours at room temperature, and extracted with ether (8 mL, 3 portions) after addition of water (10 mL). The organic portion was washed successively with water, 1N hydrochloric acid, and an aqueous saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1), to give the titled compound as a slightly brownish crystalline product (267 mg, yield: 79%),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689785B2
Source datasetuspto-grants-2004_02
ORD IDord-248343757ecb46e08ad94edae55d3d73
Source noteuspto-grants-2004_02