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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443038Generated: November 1, 2026

4-[p-Chlorobenzoyl]-1-methylpiperidine → alpha-[4-Chlorophenyl]-1-methyl-4-piperidinemethanol

https://huagongshe.com/reaction/1443038

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[p-Chlorobenzoyl]-1-methylpiperidineHCID 242680—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Productalpha-[4-Chlorophenyl]-1-methyl-4-piperidinemethanolHCID 541856100.1%

Reaction Steps

To a solution of 4-chlorophenyl 1-methylpiperidin-4-yl methanone 1.19 g (5 mmol) in 30 ml methanol was added in small portions sodium borohydride 0.378 g (10 mmol). The reaction mixture was stirred at room temperature for two hours, concentrated, added water and extracted with methylene chloride 2×50 ml. The combined organic solution was dried over sodium sulfate and concentrated to give 1.2 g of desired product in 98% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659395B2
Source datasetuspto-grants-2010_02
ORD IDord-ed72078baf4a44aab07c5473d94b7a8a
Source noteuspto-grants-2010_02