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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226905Generated: October 26, 2026

Acetone → (2-(Benzyloxy)-3-methoxyphenyl)methanol

https://huagongshe.com/reaction/2226905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant2-(Benzyloxy)-3-methoxybenzaldehydeHCID 1268087—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product(2-(Benzyloxy)-3-methoxyphenyl)methanolHCID 92725086%

Reaction Steps

A solution of 43.00 g (0.18 mole) of 2-benzyloxy-3-methoxyl-benzaldehyde of Example 1 in 300 mL of absolute ethanol is treated, with stirring, with 7.56 g (0.20 mole) of sodium borohydride. The temperature rises to 50° C. After one-half hour 10 of acetone is added, keeping the temperature at less than 60° C. with cooling. After 15 minutes the volatiles are stripped off at reduced pressure. Ice water (500 mL) is added and the product is extracted into 600 mL of ethyl acetate. The dried (Na2SO4) solution is concentrated. The remaining oil is dissolved in 100 mL of warm ether. Petroleum ether is added to turbidity to give 37.70 g (86% yield) of pure product; mp 58°-60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350757
Source datasetuspto-grants-1994_09
ORD IDord-4b720906f27b41e4828340c1b93511d9
Source noteuspto-grants-1994_09