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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982472Generated: November 1, 2026

2-Hydroxy-5-methoxybenzaldehyde → 2-(hydroxymethyl)-4-methoxyphenol

https://huagongshe.com/reaction/1982472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxy-5-methoxybenzaldehydeHCID 95695—
ReactantSodium borohydrideHCID 4311764—
ReactantDiethylether hexaneHCID 21584099—
SolventEthanolHCID 702—
Product2-(hydroxymethyl)-4-methoxyphenolHCID 48025370%

Reaction Steps

To a suspension of sodium borohydride (2.50 g, 65.8 mmol) in ethanol (100 mL) at 5° C. was added a solution of 2-hydroxy-5-methoxybenzaldehyde (10.00 g, 65.8 mmol) in ethanol (35 mL) dropwise. Upon completion of the addition the reaction mixture was allowed to stir for ten minutes then quenched by the dropwise addition of 10% aqueous acetic acid (75 mL). The ethanol was removed by concentration in vacuo and the resulting mixture poured into water (250 mL) and extracted with ethylacetate (3×100 mL). The combined extracts were washed sequentially with saturated sodium bicarbonate (50 mL), and brine (3×100 mL). The organic extract was dried (Na2SO4) and concentrated to afford a crude product (8.75 g). Trituration with hexane:ether (3:2, 25 mL) afforded 2-hydroxy-5-methoxybenzyl alcohol (7.00 g, 70%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596828
Source datasetuspto-grants-1986_06
ORD IDord-ac36c031a5964613aba1d74687b7b2f4
Source noteuspto-grants-1986_06