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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090540Generated: November 1, 2026

Hydrochloric Acid → (2S)-1-allyloxycarbonyl-2-hydroxymethyl-4-methylenepyrrolidine

https://huagongshe.com/reaction/1090540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant(2S)-1-allyloxycarbonyl-2-(t-butyldimethylsilyloxymethyl)-4-methylenepyrrolidineHCID 18639168—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product(2S)-1-allyloxycarbonyl-2-hydroxymethyl-4-methylenepyrrolidineHCID 5714933397.6%

Reaction Steps

To a solution of (2S)-1-allyloxycarbonyl-2-(t-butyldimethylsilyloxymethyl)-4-methylenepyrrolidine (2.88 g) in ethyl acetate (100 ml) was added 6N hydrochloric acid (3.0 ml) at ambient temperature. After stirring for 1 hour at ambient temperature, to the mixture were added potassium carbonate (2.54 g) and brine (30 ml) with stirring. The organic layer was separated, washed in turn with aqueous sodium hydrogen carbonate and brine, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (40 ml) eluting with a mixture of n-hexane and ethyl acetate (3:1 V/V) to give (2S)-1-allyloxycarbonyl-2-hydroxymethyl-4-methylenepyrrolidine (1.78 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081237
Source datasetuspto-grants-1992_01
ORD IDord-27574aa2f87f4c67869e37db7426cf59
Source noteuspto-grants-1992_01