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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510366Generated: October 30, 2026

Water → Ethyl 1-benzyloxycarbonyl-4-hydroxy-3-methylpyrrolidine-3-carboxylate

https://huagongshe.com/reaction/1510366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant1-Benzyl 3-ethyl 3-methyl-4-oxopyrrolidine-1,3-dicarboxylateHCID 57280137—
SolventMethanolHCID 887—
ProductEthyl 1-benzyloxycarbonyl-4-hydroxy-3-methylpyrrolidine-3-carboxylateHCID 6886127357%

Reaction Steps

To a solution of ethyl 1-benzyloxycarbonyl-3-methyl-4-oxopyrrolidine-3-carboxylate (1.0 g, 3.28 mmol) in methanol (20 mL), sodium borohydride (0.19 g, 4.92 mmol) was added at −20° C., and the mixture was stirred at the same temperature for 20 minutes. To the reaction mixture were added saturated aqueous solution of ammonium chloride (20 mL) and water (20 mL), and the mixture was extracted by ethyl acetate (20 mL×3). The extract was washed with saturated aqueous solution of sodium chloride (20 mL), and dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate, 3:1) to obtain 0.57 g (57%) of the title compound as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211910B2
Source datasetuspto-grants-2012_07
ORD IDord-66b769229c3d4443948b857532a1a4b5
Source noteuspto-grants-2012_07