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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681085Generated: November 2, 2026

Hydrochloric Acid → alpha-(4-Methoxyphenyl)-1-(2-phenylethyl)-4-piperidinemethanol hydrochloride

https://huagongshe.com/reaction/1681085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium MethoxideHCID 10942334—
Reactant(4-Methoxyphenyl)[1-(2-phenylethyl)-4-piperidinyl]-methanone hydrochlorideHCID 14257843—
SolventEthanolHCID 702—
SolventEthylacetate methanolHCID 21584119—
Productalpha-(4-Methoxyphenyl)-1-(2-phenylethyl)-4-piperidinemethanol hydrochlorideHCID 14257857—

Reaction Steps

A solution of (4-methoxyphenyl)[1-(2-phenylethyl)-4-piperidinyl]-methanone hydrochloride (3.5 g, 9.7 mmol) in absolute EtOH (75 ml) was treated with sodium methoxide (0.53 g, 9.7 mmol) followed by sodium borohydride (1.08 g, 20 mmol) and the mixture stirred for 42 h at room temperature. The reaction mixture was filtered and the filtrate concentrated to a solid residue which was dissolved in absolute Et2O and treated with HCl (9.7 mmol) dissolved in CH3OH/EtOAc (1:3, 8 ml). The resulting precipitate was filtered and recrystallized from CH3OH/Et2O to give alpha-(4-methoxyphenyl)-1-(2-phenylethyl)-4-piperidinemethanol hydrochloride, mp 162.5°-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169096
Source datasetuspto-grants-1992_12
ORD IDord-5279af027eb64ee192bbe0c8ec440244
Source noteuspto-grants-1992_12