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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260081Generated: October 25, 2026

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

https://huagongshe.com/reaction/260081

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-methoxy-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 mL 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 numberUS05525614
Source datasetuspto-grants-1996_06
ORD IDord-f760b7f1e7ff433698dbe74588dcb3ae
Source noteuspto-grants-1996_06