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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034431Generated: October 30, 2026

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

https://huagongshe.com/reaction/1034431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantPiperidineHCID 8082—
ReactantBoric acid (H3BO3), disodium saltHCID 14496929—
SolventMethanolHCID 887—
Product1-(3-Hydroxybenzyl)piperidineHCID 82697485%

Reaction Steps

3-Hydroxybenzaldehyde (III) (0.246 mol, 30 g) was dissolved into 150 ml of methanol. Piperidine (IV) (0.6 mol, 52 g) was added to the solution and the mixture was stirred at room temperature to dissolution. To the solution was added under ice cooling sodium hydrogen borate (0.247 mol, 9.4 g) while stirring over 1 hour, followed by continued stirring for 1 hour at room temperature. The reaction mixture was concentrated under vacuum. The residue was dissolved in 200 ml of 3N hydrochloric acid and washed twice with 50 ml of ethyl acetate. The water layer was alkalinized (pH 10) with about 50 ml of concentrated aqueous ammonia to deposit crystals. The crystals were collected by filtration, washed with water, dried under vacuum, and recrystallized from a mixed solvent of acetone and n-hexane, to obtain 40 g of 3-piperidinomethylphenol (V) (yield: 84.7%). m.p. 135°-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05317026
Source datasetuspto-grants-1994_05
ORD IDord-a5d0e33bec5c4f7e9d41c668ec775573
Source noteuspto-grants-1994_05