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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441415Generated: October 30, 2026

4-Hydroxybenzyl Alcohol → 2-(4-Phenoxymethylphenoxy)-propionic acid

https://huagongshe.com/reaction/441415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantPhenolHCID 996—
ReactantEthyl 2-bromopropionateHCID 79040—
Reactant2-[4-(Hydroxymethyl)phenoxy]propanoic acidHCID 351924—
ReactantSodiumHCID 5360545—
Reactant2-(p-Bromoethylphenoxy)-propionic acidHCID 57189959—
SolventEthanolHCID 702—
Product2-(4-Phenoxymethylphenoxy)-propionic acidHCID 21421173—

Reaction Steps

2.3 g. of sodium is dissolved in 250 ml. of absolute ethanol; 9.4 g. of phenol and 28.6 g. of the ethyl ester of 2-(p-bromoethylphenoxy)-propionic acid [obtainable by reacting p-hydroxybenzyl alcohol with ethyl 2-bromopropionate to the ethyl ester of 2-(p-hydroxymethylphenoxy)-propionic acid and subsequent reaction with SOBr2 ] are added thereto, and the mixture is refluxed for 3 hours and evaporated. The usual working-up procedure yields the ethyl ester of 2-(4-phenoxymethylphenoxy)-propionic acid. Analogously, the ethyl ester of 2-(4-phenoxymethylphenoxy)-2-methylpropionic acid is obtained from the ethyl ester of 2-p-bromomethylphenoxyisobutyric acid (obtainable by bromination of the ethyl ester of 2-p-methylphenoxyisobutyric acid with N-bromosuccinimide);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04039683
Source datasetuspto-grants-1977_08
ORD IDord-61e8a8cd51c44809b1f1726acb960e76
Source noteuspto-grants-1977_08