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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039214Generated: November 3, 2026

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

https://huagongshe.com/reaction/2039214

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 numberUS08575118B2
Source datasetuspto-grants-2013_11
ORD IDord-8ec29ef67924438cb01120e429147c5f
Source noteuspto-grants-2013_11