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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601718Generated: October 25, 2026

Allyl chloroformate → Allyl-3-methanesulphonyloxy-pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1601718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chloroformateHCID 18052—
Reactant(S)-1-Benzyl-3-mesyloxypyrrolidineHCID 10934081—
ReactantMethanol--water (1/1)HCID 22242641—
SolventHeptaneHCID 8900—
ProductAllyl-3-methanesulphonyloxy-pyrrolidine-1-carboxylateHCID 21832213—

Reaction Steps

6.4 ml of allyl chloroformate were added dropwise to 10.2 g of methanesulphonic acid (S)-1-benzyl-pyrrolidin-3-yl ester in 880 ml of n-heptane at room temperature within 10 minutes under argon and with slight cooling. The two-phase mixture was stirred vigorously for 2 hours 45 minutes and subsequently treated with 40 ml of methanol/water (1:1). The aqueous methanolic phase was separated, extracted with 40 ml of heptane and thereafter the methanol was distilled off on a rotary evaporator. The aqueous phase was extracted twice with 30 ml of ethyl acetate. The organic phases were combined, dried over Na2SO4, filtered and the filtrate was concentrated. 8.23 g of beige oil were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977381
Source datasetuspto-grants-1999_11
ORD IDord-3ae0e8dbf1aa4eb39309ecb2fee6b00a
Source noteuspto-grants-1999_11