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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439212Generated: October 25, 2026

Ethyl bromoacetate → 4(4-Fluorobenzoyl)-2,3-dichlorophenoxy acetic acid

https://huagongshe.com/reaction/1439212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium HydroxideHCID 14798—
ReactantSodiumHCID 5360545—
Reactant2,3-Dichloro-4-hydroxy-4'-fluorobenzophenoneHCID 13015707—
SolventEthanolHCID 702—
Product4(4-Fluorobenzoyl)-2,3-dichlorophenoxy acetic acidHCID 20393689—

Reaction Steps

Into a solution of 1.4 g. (0.06 g. atom) of sodium in 200 ml. of absolute alcohol, 16.0 g. (0.056 mole) of 4(4-fluorobenzoyl)-2,3-dichlorophenol was added and the mixture was stirred for thirty minutes at room temperature. The excess of alcohol was vacuum removed and the residue was washed with ether to obtain the sodium salt. The sodium salt of 4(4-fluorobenzoyl)-2,3-dichlorophenol was dissolved in 200 ml. of ethanol and 10.5 g. (0.06 mole) of ethyl bromoacetate was added and the reaction mixture was refluxed for 16 hours, filtered and the solvent was removed in vacuo. The residue was triturated with pet. ether and filtered to obtain a solid product. The product obtained was dissolved in 150 ml. ethanol and 50 ml. of 20% NaOH aqueous solution was added. The reaction mixture was refluxed for 1/2 hour and the solvent was partially removed in vacuo. The residue was dissolved in hot water and filtered. The hot filtrate was acidified with concentrated hydrochloric acid at 60° C. The resulting precipitate was collected by filtration and washed with water. Recrystallization from dichloroethane afforded 8.0 g. (47%) of the product; m.p. 174°-176°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04058559
Source datasetuspto-grants-1977_11
ORD IDord-6ac66464c7f2430fa32bf5967840c17a
Source noteuspto-grants-1977_11