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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323333Generated: October 30, 2026

Sodium borohydride → (3-(Pyrid-3-yl)-5-oxo-pyrrolidin-3-yl)acetic acid ethyl ester

https://huagongshe.com/reaction/323333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantDichloromethane methanolHCID 21226129—
Reactant3-cyano-3-(pyrid-3-yl)pentanedioic Acid Diethyl EsterHCID 54182890—
CatalystDichlorocobalt hexahydrateHCID 517166—
SolventMethanolHCID 887—
Product(3-(Pyrid-3-yl)-5-oxo-pyrrolidin-3-yl)acetic acid ethyl esterHCID 22009411—

Reaction Steps

Combine 3-cyano-3-(pyrid-3-yl)pentanedioic acid diethyl ester (50 g, 172 mmol) and cobalt(II)chloride hexahydrate (81.8 g, 344 mmol) in methanol (500 mL). While maintaining the temperature at or below 20° C. with an ice-bath, add portionwise sodium borohydride (65.1 g, 1.72 mol). After the addition is complete, allow the reaction mixture to stand at ambient temperature. After 18 hours, evaporate the reaction mixture in vacuo to obtain a residue. Quench the reaction mixture by adding ammonium chloride and 0.5 M aqueous sodium hydroxide solution. Adjust the pH of the quenched reaction mixture to about 8 using 1 M aqueous hydrochloric acid solution. Filter through celite and extract the aqueous filtrate twice with dichloromethane. Combine the organic layers, dry over Na2SO4, filter, and concentrate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with dichloromethane/methanol 10/1 to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-04ef77d8212345dbbfa5064ff0ab3354
Source noteuspto-grants-2001_04