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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185879Generated: November 1, 2026

Methyl chloroformate → (S)-benzyl 4-(difluoromethoxy)-2-(methoxycarbonylamino)butanoate

https://huagongshe.com/reaction/1185879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
Reactant(S)-benzyl 2-amino-4-(difluoromethoxy)butanoateHCID 67991507—
SolventDichloromethaneHCID 6344—
Product(S)-benzyl 4-(difluoromethoxy)-2-(methoxycarbonylamino)butanoateHCID 5961062340%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-Benzyl 2-amino-4-(difluoromethoxy)butanoate (116 mg, 0.448 mmol) was dissolved in anhydrous dichloromethane (2.5 mL) and cooled down to 0° C. and TEA (181 mg, 1.79 mmol) and methylchloroformate (51 mg, 0.538 mmol) were added respectively. The mixture was stirred for 30 minutes and then it was stirred at room temperature overnight. The resulting product mixture was quenched with saturated NaHCO3 and extracted with dichloromethane. The organic layer was washed with saturated NH4Cl solution and brine and dried over Na2SO4. The volatiles were removed in vacuo to afford 56 mg (40%) of desired product after column purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669234B2
Source datasetuspto-grants-2014_03
ORD IDord-f0d4f6d85c0e4f479e305d36d04e3cc8
Source noteuspto-grants-2014_03