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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434591Generated: October 28, 2026

Sodium borohydride → HCID 68704632, compound

https://huagongshe.com/reaction/1434591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57935976HCID 57935976—
SolventEthanolHCID 702—
ProductHCID 68704632HCID 68704632—

Reaction Steps

Sodium borohydride (189 mg) was added to a solution of 3-{4-[5-(methylsulfonyl)-1H-benzimidazol-1-yl]piperidin-1-yl}-1-phenylpropan-1-one (2.07 g) in ethanol (40 ml) at 0° C., the mixture was allowed to warm to room temperature and was stirred for 16 hours. The reaction mixture was evaporated to dryness, the residue was redissolved in dichloromethane and washed with water (15 ml) and brine (15 ml) and dried. Removal of the solvent gave 3-{4-[5-(methylsulfonyl)-1H-benzimidazol-1-yl]piperidin-1-yl}-1-phenylpropan-1-ol, 2.1 g, M+H 414.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615555B2
Source datasetuspto-grants-2009_11
ORD IDord-3ae6950eaf34440caacf3571db161d47
Source noteuspto-grants-2009_11