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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609457Generated: November 1, 2026

3-Hydroxybenzaldehyde → 1-(3-Hydroxybenzyl)piperidine

https://huagongshe.com/reaction/1609457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantPiperidineHCID 8082—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product1-(3-Hydroxybenzyl)piperidineHCID 82697455.5%

Reaction Steps

In 800 ml of ethanol was dissolved 122 g of 3-hydroxybenzaldehyde and thereto was gradually added 210 g of piperidine. To the mixture was added 38 g of sodium borohydride under cooling with ice and the mixture was stirred for 8 hours at room temperature. The resulting mixture was concentrated at a reduced pressure. To a residue were added ice-cold water and hydrochloric acid to render a solution acidic. The solution was washed with diethyl ether. An aqueous layer was made alkaline with addition of sodium carbonate and then extracted with ethyl acetate. After removing the solvent, 106 g (yield 55%) of 3-(1-piperidinomethyl)phenol was obtained in the form of white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401739
Source datasetuspto-grants-1995_03
ORD IDord-2f8a856fac894105b1de49b3d7882367
Source noteuspto-grants-1995_03