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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129594Generated: October 25, 2026

3-Hydroxybenzyl alcohol → 2-(3-Hydroxymethylphenoxy)phenylacetic acid

https://huagongshe.com/reaction/129594

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxybenzyl alcoholHCID 102—
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromophenylacetic acidHCID 87754—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(3-Hydroxymethylphenoxy)phenylacetic acidHCID 15125737130.1%

Reaction Conditions

Temperature140 °C

Reaction Steps

3-Hydroxybenzyl alcohol (31.0 g) was ground finely and stirred with potassium carbonate (34.6 g), 2-bromophenylacetic acid (26.9 g) and cuprous chloride (large spatula full) under nitrogen. The mixture was warmed to 140° C., and stirred vigorously for 31/2 hours. DMF (60 ml) was then added to the stirred melt and the solution was allowed to cool, poured into water and acidified with dilute hydrochloric acid. The aqueous layer was extracted with ether, and the ether extracts were washed with water, dried and evaporated to give 2-(3-hydroxymethylphenoxy)phenylacetic acid as a brown oil (42.03 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468857
Source datasetuspto-grants-1995_11
ORD IDord-ccde36f6580d4ba39e2922e675ab5822
Source noteuspto-grants-1995_11