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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267193Generated: October 25, 2026

Potassium borohydride → 4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanol

https://huagongshe.com/reaction/267193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium borohydrideHCID 4192641—
ReactantSodium MethoxideHCID 10942334—
Reactant4-[4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]piperidino]butyrophenone hydrochlorideHCID 21555731—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanolHCID 21555715—

Reaction Steps

To a mixture of 4.2 g (0.0083 mole) of 4-[4-[α-(p tert-butylphenyl)-α-hydroxybenzyl]piperidino]butyrophenone hydrochloride and 0.54 g (0.01 mole) of sodium methoxide in 25 ml of methanol is added 2.16 g (0.04 mole) of potassium borohydride. The reaction mixture is stirred overnight, diluted with water and the methanol removed under reduced pressure. The remaining material is extracted with chloroform, washed with water, dried over magnesium sulfate and filtered. The filtrate is concentrated, and the residue is recrystallized from acetone-water to give 4-[α-(p-tert-butylphenyl)-α-hydroxybenzyl]-α-phenyl-1-piperidinebutanol, M.P. 161°-163°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03941795
Source datasetuspto-grants-1976_03
ORD IDord-31d54994f1804563936e334fbdce7530
Source noteuspto-grants-1976_03