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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343491Generated: October 31, 2026

Sodium borohydride → (3-(3,4-Dimethoxyphenyl)-5-oxopyrrolidin-3-yl)acetic acid ethyl ester

https://huagongshe.com/reaction/343491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Cyano-3-(3,4-dimethoxyphenyl)pentanedioic diethyl esterHCID 15392019—
ReactantEthylacetate methanolHCID 21584119—
CatalystDichlorocobalt hexahydrateHCID 517166—
SolventMethanolHCID 887—
Product(3-(3,4-Dimethoxyphenyl)-5-oxopyrrolidin-3-yl)acetic acid ethyl esterHCID 15392020—

Reaction Steps

Combine 3-cyano-3-(3,4-dimethoxyphenyl)pentanedioic diethyl ester (1.3 g, 3.24 mmol) and cobalt(II)chloride hexahydrate (1.54 g, 6.48 mmol) in methanol (50 mL). While maintaining the temperature at or below 20° C. with an ice-bath, add portionwise sodium borohydride (2.17 g, 57 mmol). After the addition is complete, allow the reaction mixture to stand at ambient temperature for 18 hours. Evaporate the reaction mixture invacuo to obtain a residue. Partition the residue between dichloromethane and 1M hydrochloric acid solution. Extract the aqueous layer several times with dichloromethane, combine the organic layers, dry over Na2SO4, filter, and concentrate invacuo to obtain a residue. Chromatograph the residue on silica gel eluting with 20/1 ethyl acetate/methanol. Remove residual solvent inuacuo at 82° C. to give the title compound: Rf= 0.74 (silica gel, 5/1 ethyl acetate/methanol); mp; 116°-118° C. Elemental Analysis calculated for C16H21NO5 : C 62.53; H 6.89; N 4.56; Found: C 62.52; H 6.85; N 4.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861417
Source datasetuspto-grants-1999_01
ORD IDord-0f26e558cca24a468db03bd81fe9ce8e
Source noteuspto-grants-1999_01