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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613993Generated: October 30, 2026

Hydrochloric Acid → (2S,4R)-1-allyloxycarbonyl-4-hydroxy-2-hydroxymethylpyrrolidine

https://huagongshe.com/reaction/1613993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant(2S,4R)-1-allyloxycarbonyl-2-methoxycarbonyl-4-hydroxypyrrolidineHCID 10633157—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product(2S,4R)-1-allyloxycarbonyl-4-hydroxy-2-hydroxymethylpyrrolidineHCID 15086219108%

Reaction Conditions

Temperature27.5 °C

Reaction Steps

To a solution of (2S,4R)-1-allyloxycarbonyl-4-hydoxy2-methoxycarbonylpyrrolidine (10 g) in tetrahydrofuran (20 ml) and ethanol (30 ml) was added by portions sodium borohydride (3.30 g) with stirring at 25-30° C., and the mixture was stirred at the same temperature for 4 hours. To the reaction mixture was added dropwise conc. hydrochloric acid (7.27 ml) with stirring at 0-2° C. The resulting precipitates were filtered off and the filtrate was evaporated in vacuo. The resulting residue was dissolved in a mixture of tetrahydrofuran (20 ml), ethanol (20 ml) and saturated aqueous sodium chloride (50 ml). The organic layer was evaporated in vacuo to give (2S,4R)-1-allyloxycarbonyl-4-hydroxy-2-hydroxymethylpyrrolidine (9.48 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194624
Source datasetuspto-grants-1993_03
ORD IDord-38e2bf1d102f4c5e8dc4a5901bfa2f48
Source noteuspto-grants-1993_03