Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367461Generated: October 30, 2026

Sodium borohydride → HCID 66918731, compound

https://huagongshe.com/reaction/1367461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66918396HCID 66918396—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66918731HCID 66918731—

Reaction Steps

To a solution of (1R,2R)-2-(1-cyano-cyclopropylcarbamoyl)-4-oxo-cyclopentanecarboxylic acid ethyl ester (0.38 mmol) in THF (2.0 ml) was added at −15° C. sodium borohydride (0.38 mmol) and stirring was continued for 4 h. The mixture was partitioned between 1N aqueous HCl and ethyl acetate, the organic layer was dried, evaporated and the residue chromatographed on silica using ethyl acetate to give (1R,2R)-2-(1-cyano-cyclopropylcarbamoyl)-4-hydroxy-cyclopentanecarboxylic acid ethyl ester as a 2:1 mixture of epimers as a colorless solid. MS: 267.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893099B2
Source datasetuspto-grants-2011_02
ORD IDord-e54ae8711ab24ffabb0319038fdc0411
Source noteuspto-grants-2011_02