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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043111Generated: November 1, 2026

Water → (3-chloro-4-fluorophenoxy)acetic acid

https://huagongshe.com/reaction/2043111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl bromoacetateHCID 60984—
Reactant3-Chloro-4-fluorophenolHCID 75790—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
Product(3-chloro-4-fluorophenoxy)acetic acidHCID 22307079.1%

Reaction Steps

To a stirring solution of finely ground KOH (1.2 g, 20.4 mmol) in DMSO (6 mL) was added 3-chloro-4-fluorophenol (1.0 g, 6.8 mmol). The mixture was stirred for 10 minutes at RT, then cooled to 0° C. Methyl bromoacetate (1.25 g, 8.2 mmol) was added, and the reaction was slowly warmed to RT and stirred overnight. H2O (10 mL) and MeOH (10 mL) were added to the mixture, and the reaction was stirred for 1 h. After removing MeOH under reduced pressure, H2O (100 mL) and Et2O (50 mL) were added, and the layers were separated. The aqueous phase was acidified to pH 2 with an aqueous concentrated HCl solution and extracted with CH2Cl2 (200 mL). The organic layer was dried over MgSO4, filtered, concentrated, and dried to give 2-(3-chloro-4-fluorophenoxy)acetic acid as a white solid (1.1 g, 79%). 1H NMR (400 MHz, CDCl3) δ 7.10 (t, J=8.8 Hz, 1H), 7.01-6.98 (m, 1H), 6.84-6.80 (m, 1H), 4.68 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586589B2
Source datasetuspto-grants-2013_11
ORD IDord-cc67523c58214243b52efd6175feb43e
Source noteuspto-grants-2013_11