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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414571Generated: October 27, 2026

Guaiacol → 5-Chloro-2-(2'-methoxyphenoxy)benzoic acid

https://huagongshe.com/reaction/1414571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuaiacolHCID 460—
Reactant2,5-Dichlorobenzoic acidHCID 5784—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
CatalystCopperHCID 23978—
SolventMethanolHCID 887—
Product5-Chloro-2-(2'-methoxyphenoxy)benzoic acidHCID 23460522—

Reaction Steps

A mixture of 2,5-dichlorobenzoic acid (9.5 g.), 2-methoxyphenol (7.4 g.) and copper bronze (1.0 g.) is added to a solution of sodium methoxide in methanol prepared from sodium (2.53 g.) and methanol (50 ml.). The excess methanol is evaporated and 1,2-dichlorobenzene (50 ml.) is added to the residue. The mixture is stirred and heated under reflux for 2.5 hours. The mixture is cooled, acidified with 3N hydrochloric acid, filtered to remove copper bronze and extracted with chloroform. The organic layer is separated and extracted with saturated sodium hydrogen carbonate solution. The sodium hydrogen carbonate extract is acidified. The precipitate is filtered off, dissolved in toluene, and the toluene solution treated with carbon, filtered and the solvent evaporated. The solid residue is recrystallised from toluene-petroleum ether (b.p. 60°-80° C.) to give 5-chloro-2-(2'-methoxyphenoxy)benzoic acid, m.p. 115°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001419
Source datasetuspto-grants-1977_01
ORD IDord-a5c8a006789446f0b0b26cf189c3d0d1
Source noteuspto-grants-1977_01