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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941623Generated: November 2, 2026

Sulfuric Acid → (2S,4R)-1-allyloxycarbonyl-4-methanesulfonyloxypyrrolidine-2-methanol

https://huagongshe.com/reaction/1941623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium borohydrideHCID 4311764—
Reactant(2S,4R)-N-allyloxycarbonyl-4-methanesulfonyloxyproline methyl esterHCID 10733517—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product(2S,4R)-1-allyloxycarbonyl-4-methanesulfonyloxypyrrolidine-2-methanolHCID 1863917293.5%

Reaction Steps

To a solution of (2S,4R)-1-allyloxycarbonyl-4-methanesulfonyloxy-2-methoxycarbonylpyrrolidine (27.12 g: 74.0 mmole) in a mixture of tetrahydrofuran (94 ml) and ethanol (140 ml), sodium borohydride (12 g: 31.7 mmole) is added in a nitrogen atmosphere under ice cooling. The mixture is stirred for 4 hours at room temperature. To the reaction mixture concentrated sulfuric acid (8.8 ml: 158.4 mmole) is added dropwise under ice cooling. The reaction mixture is concentrated to half a volume in vacuo, and diluted with ethyl acetate (100 ml) and ice water (100 ml). The organic layer is taken, successively washed with aqueous sodium hydrogen carbonate and saturated brine, dried over magnesium sulfate, and concentrated in vacuo to give (2S,4R)-1-allyloxycarbonyl-4-methanesulfonyloxypyrrolidine-2-methanol (19.33 g). Yield: 77%. Colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703243
Source datasetuspto-grants-1997_12
ORD IDord-32418fb7d7ab40ef8df1d48e565efa43
Source noteuspto-grants-1997_12