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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375093Generated: November 3, 2026

Sodium borohydride → HCID 69417629, compound

https://huagongshe.com/reaction/1375093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86590648HCID 86590648—
SolventEthanolHCID 702—
ProductHCID 69417629HCID 69417629100.3%

Reaction Steps

A stirred suspension of [1-(4-{(benzotriazol-1-ylmethyl)-amino}-phenyl)-cyclopentyl]-acetic acid tert-butyl ester (0.21 g) in ethanol (10 mL), under argon, was treated with sodium borohydride (0.051 g). After stirring at room temperature for 2 hours a further aliquot of sodium borohydride (0.017 g) was added and stirring was continued for a further hour, then a further aliquot of sodium borohydride (0.017 g) was added and stirring was continued for a further hour. The reaction mixture was then evaporated and the residue was treated with water (15 mL) and ethyl acetate (25 mL). The organic phase was separated and then washed with water (15 mL), then with brine (15 mL), then dried over magnesium sulfate and then evaporated to give the title compound (0.15 g) as an amber oil which crystallised on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166616B2
Source datasetuspto-grants-2007_01
ORD IDord-4f0d6d84fe434e1cad382bd17dcbb38a
Source noteuspto-grants-2007_01