Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198629Generated: October 30, 2026

HCID 14519886, compound → HCID 14519887, compound

https://huagongshe.com/reaction/1198629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14519886HCID 14519886—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 14519887HCID 14519887—

Reaction Steps

A solution of crude 2-(4-methyl-2-phenylmethoxyphenyl)acetonitrile (15 g, 63 mmol) in ethanol (200 ml) and water (50 ml) containing 10 g (0.25 mol) NaOH was heated under reflux overnight, and the ethanol was removed under vacuum. The residue was diluted with water and washed with benzene. The aqueous layer was then acidified with dilute HCl to give an oil which was extracted into ethyl acetate to give (4-methyl-2-phenylmethoxyphenyl)acetic acid (14.2 g, 88%) as an oil which solidified on standing. A solution of this crude (4-methyl-2-phenylmethoxyphenyl)acetic acid in ethanol was hydrogenated over palladium on charcoal to give (2-hydroxy-4-methylphenyl)acetic acid. Anal (C9H10O3) C,H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281620
Source datasetuspto-grants-1994_01
ORD IDord-c8eb050728ad4917ba80d15c2f51a585
Source noteuspto-grants-1994_01