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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029650Generated: October 31, 2026

Water → (2R,4S)-1-(tert-butoxycarbonyl)-4-cyano-2-methylpyrrolidine

https://huagongshe.com/reaction/1029650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium CyanideHCID 8929—
ReactantHCID 22843271HCID 22843271—
SolventDimethyl SulfoxideHCID 679—
Product(2R,4S)-1-(tert-butoxycarbonyl)-4-cyano-2-methylpyrrolidineHCID 2284327271.6%

Reaction Steps

A solution of (2R,4R)-1-(tert-butoxycarbonyl)-4-methanesulfonyloxy-2-methylpyrrolidine (2.3 g) and sodium cyanide (1.37 g) in dimethyl sulfoxide (25 ml) was heated for two and a half hours at 90° C. The reaction mixture was poured into a mixture of water (100 ml) and ethyl acetate (100 ml). The organic layer was separated, washed with brine, and dried over magnesium sulfate. Evaporation of the solvent gave an oil, which was chromatographed on silica gel (100 ml) eluting with a mixture of hexane and ethyl acetate (4:1, V/V) to give (2R,4S)-1-(tert-butoxycarbonyl)-4-cyano-2-methylpyrrolidine (1.24 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102877
Source datasetuspto-grants-1992_04
ORD IDord-966eb4f04b4543ff9af49453e34365f5
Source noteuspto-grants-1992_04