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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380289Generated: November 1, 2026

Acetic Acid → 1-[(3,4-Dimethoxyphenyl)methyl]-4-(hydroxymethyl)pyrrolidin-2-one

https://huagongshe.com/reaction/1380289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBorohydrideHCID 28123—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 1-[(3,4-dimethoxyphenyl)methyl]-5-oxo-3-pyrrolidinecarboxylateHCID 13422554—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-[(3,4-Dimethoxyphenyl)methyl]-4-(hydroxymethyl)pyrrolidin-2-oneHCID 13422557—

Reaction Steps

8.0 g of 1-(3,4-dimethoxybenzyl)-4-ethoxycarbonyl-pyrrolidin-2-one were dissolved in 100 ml of methanol. Over a period of 20 minutes, at 0°-10° C., a solution of 2.8 g of sodium borohydride in 30 ml of water was added dropwise, while mechanically stirring, and the mixture was stirred for 5 hours more at 0°-10° C. The excess borohydride was then carefully decomposed by the addition of glacial acetic acid up to a pH of 5 and until the development of gas had ceased, and the methanol was distilled off in vacuo. Some water was added, and the reaction product was taken up in methylene chloride. The methylene chloride phase was then washed with water, dried and evaporated. The residue was chromatographed on silica gel (eluant: methylene chloride/methanol 98:2). Finally, 4.8 g (62% of theory) of the title compound were obtained from the eluate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581364
Source datasetuspto-grants-1986_04
ORD IDord-a9d8524d261a4800a0950f92f3ddbf09
Source noteuspto-grants-1986_04