Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703593Generated: October 30, 2026

Sodium Hydroxide → (2S,4R)-1-allyloxycarbonyl-2-(2-hydroxyethyloxymethyl)-4-methanesulfonyloxypyrrolidine

https://huagongshe.com/reaction/703593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAllyl chloroformateHCID 18052—
Reactant(2S,4R)-2-(2-hydroxyethyloxymethyl)-4-methanesulfonyloxypyrrolidineHCID 57005235—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2S,4R)-1-allyloxycarbonyl-2-(2-hydroxyethyloxymethyl)-4-methanesulfonyloxypyrrolidineHCID 18642540—

Reaction Steps

To a solution of (2S,4R)-2-(2-hydroxyethyloxymethyl)-4-methanesulfonyloxypyrrolidine (30.5 g) in a mixture of tetrahydrofuran (120 ml) and water (120 ml) was dropwise added a solution of allyl chloroformate (14.5 ml) in tetrahydrofuran (14.5 ml) under ice-cooling with stirring, keeping the pH between 9-10 with 4N aqueous sodium hydroxide. The mixture was stirred at the same condition for one hour and extracted with ethyl acetate (200 ml). The organic layer was dried over magnesium sulfate and evaporated under reduced pressure to give a syrup. The syrup was subjected to a column chromatography on silica gel (400 g) and eluted with a mixture of methanol and dichloromethane (2:98 V/V) to give (2S,4R)-1-allyloxycarbonyl-2-(2-hydroxyethyloxymethyl)-4-methanesulfonyloxypyrrolidine (28.03 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983596
Source datasetuspto-grants-1991_01
ORD IDord-efadcddc7adb4068bc4be1919a611ca3
Source noteuspto-grants-1991_01