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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419622Generated: October 26, 2026

Ethanol → Benzoic acid, 2,4-dichloro-5-fluoro-, ethyl ester

https://huagongshe.com/reaction/1419622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2,4-Dichloro-5-fluorobenzoyl chlorideHCID 2736821—
SolventDiethyl EtherHCID 3283—
ProductBenzoic acid, 2,4-dichloro-5-fluoro-, ethyl esterHCID 1363072290.8%

Reaction Conditions

Temperature17 °C

Reaction Steps

A 25-mL round-bottom flask was equipped with a magnetic stir bar, thermometer, nitrogen inlet, addition funnel, and a reflux condenser. The flask was charged with 2,4-dichloro-5-fluorobenzoyl chloride (5.38 g, 23.65 mmol) and ethyl ether (5.0 g). The resulting colorless solution was cooled to 17° C. using a cool water bath. Ethanol (3.20 g, 69.47 mmol; absolute grade) was added dropwise from the addition funnel over ten minutes. Once the addition was complete, the solution was warmed to room temperature and stirred overnight (17 hours). Additional ether (20 mL) was added to the reaction mixture, which was then transferred to a separatory funnel. The reaction mixture was washed twice with 2% sodium hydroxide solution (10 mL), then with water (10 mL). The upper organic layer was separated and dried over sodium sulfate. The solvent was removed by evaporation under reduced pressure. The residue was dried in a vacuum oven to give 5.09 g of ethyl 2,4-dichloro-5-fluorobenzoate as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886210
Source datasetuspto-grants-1999_03
ORD IDord-58ddac9ecb2b4652b575a9e3beaa407b
Source noteuspto-grants-1999_03