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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700246Generated: October 26, 2026

Ethyl bromoacetate → (2,6-Dichloro-4-fluorophenoxy)acetic acid

https://huagongshe.com/reaction/1700246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenol, 2,6-dichloro-4-fluoro-HCID 94950—
SolventAcetoneHCID 180—
Product(2,6-Dichloro-4-fluorophenoxy)acetic acidHCID 22306772.8%

Reaction Steps

The mixture of 2,6-dichloro-4-fluorophenol (362 mg, 2.0 mmol), potassium carbonate (910 mg, 6.6 mmol), ethyl bromoacetate (500 mg, 3.0 mmol) and acetone (25 ml) was refluxed for 12 h. After cooling, the mixture was filtered to remove potassium carbonate. The filtrate was concentrated under reduced pressure. To this residue, 10 ml dioxane and 14 ml 5% sodium hydroxide solution were added. After the mixture was stirred at room temperature overnight, it was acidified with concentrated hydrochloric acid to pH 2, and then extracted three times with ethyl acetate (15 ml each). Organic phases were combined, washed with water and brine, dried over magnesium sulfate, filtered, and then evaporated in vacuo. The residue was recrystallized from ethyl acetate and petroleum ether to give 348 mg 2,6-dichloro-4-fluorophenoxyacetic acid as white crystals, mp 155-158° C., yield: 72.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350756B1
Source datasetuspto-grants-2002_02
ORD IDord-3672876408014063af8e23098d88aab8
Source noteuspto-grants-2002_02