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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11614Generated: October 27, 2026

Bromide ion → (4-Chloro-2-hydroxyphenoxy)acetic acid

https://huagongshe.com/reaction/11614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant2-(4-Chloro-2-methoxyphenoxy)acetic acidHCID 11658584—
SolventWaterHCID 962—
Product(4-Chloro-2-hydroxyphenoxy)acetic acidHCID 16748825—

Reaction Steps

To a solution of 48% aqueous hyrdrogen bromide (20 mL) was added (4-chloro-2-methoxy-phenoxy)-acetic acid (2.1 g, 9.7 mmol). The resulting mixture was heated to reflux overnight. The mixture was cooled to ambient temperature, diluted with water and extracted with diethyl ether. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo to give (4-chloro-2-hydroxy-phenoxy)-acetic acid. The crude product was added to a solution of pyridinium p-toluene sulfonate (0.10 g, 0.40 mmol) in toluene (100 mL). The resulting mixture was heated to reflux for five hours. The reaction was allowed to cool to ambient temperature and concentrated in vacuo. Chromatography on silica gel gave the title compound (0.97 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098212B2
Source datasetuspto-grants-2006_08
ORD IDord-a62f0d2dcbcb40f2a0c77212a8c65747
Source noteuspto-grants-2006_08