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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525144Generated: November 2, 2026

Chloroacetic Acid → 2-(2-Acetyl-4-bromophenoxy)acetic acid

https://huagongshe.com/reaction/525144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantSodium HydroxideHCID 14798—
Reactant5'-Bromo-2'-hydroxyacetophenoneHCID 95991—
SolventWaterHCID 962—
Product2-(2-Acetyl-4-bromophenoxy)acetic acidHCID 19261363—

Reaction Steps

A solution of 1-(5-bromo-2-hydroxyphenyl)ethanone (9.53 mmol) in water (70 mL) was treated with chloroacetic acid (11.64 mmol) and a solution of NaOH (21.25 mmol) in water (20 mL). The resulting yellow suspension was flushed with N2 and stirred at reflux overnight. Analysis by LCMS indicated the consumption of starting material and desired product formation. The reaction was cooled to room temperature and then acidified to pH˜3 with 1N aq HCl. The mixture was then cooled to 0° C. resulting in precipitate formation. A grey sticky solid was filtered and used without further purification. MS(ES)+ m/e 273/275 [M+H]+ (bromide isotope pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340529B2
Source datasetuspto-grants-2016_05
ORD IDord-354e11f1fb0b45a3a03f23def3a8f90a
Source noteuspto-grants-2016_05