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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047381Generated: October 25, 2026

Sodium borohydride → 1-[3-(1H-Benzoimidazol-2-yl)-4-chloro-phenyl]-piperidin-4-ol

https://huagongshe.com/reaction/2047381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-[3-(1H-benzo[d]imidazol-2-yl)-4-chlorophenyl]piperidin-4-oneHCID 59568243—
SolventMethanolHCID 887—
Product1-[3-(1H-Benzoimidazol-2-yl)-4-chloro-phenyl]-piperidin-4-olHCID 5956836936%

Reaction Steps

To a suspension of 1-[3-(1H-benzoimidazol-2-yl)-4-chloro-phenyl]-piperidin-4-one (0.05 g, 0.17 mmol) in methanol (50 mL) was added sodium borohydride (NaBH4) (0.01 g, 0.17 mmol) and the resulting mixture was stirred for 1 h at room temperature and then quenched with few drops of water. The solvent was removed under reduced pressure, the crude dissolved in EtOAc (5 mL) and filtered, then the organic phase was evaporated under reduced pressure to afford 0.02 g (36%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592463B2
Source datasetuspto-grants-2013_11
ORD IDord-b68508f9a2104c64b457a0df3cd08835
Source noteuspto-grants-2013_11