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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845810Generated: October 31, 2026

Phenol → Phenyl 2,4,5-trifluorobenzoate

https://huagongshe.com/reaction/1845810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4,5-Trifluorobenzoyl chlorideHCID 145164—
SolventDichloromethaneHCID 6344—
ProductPhenyl 2,4,5-trifluorobenzoateHCID 10354819—

Reaction Steps

A solution of phenol (13.3 g, 141 mmol) in dry dichloromethane (370 mL) was cooled in ice bath and treated with N,N-diisopropylethylamine (34 mL, 193 mmol) followed by dropwise addition of 2,4,5-trifluorobenzoyl chloride (25 g, 129 mmol) over a period of 15 minutes. The ice bath was removed, stirring was continued for two hours at room temperature and the solution was then transferred to a separatory funnel and the organic layer was washed successively with hydrochloric acid solution (2N, 150 mL), saturated aqueous sodium bicarbonate solution (150 mL), and brine (150 mL), dried over anhydrous sodium sulfate, filtered, evaporated and the resulting solid product was purified on silica in portions by eluting successively with hexane, and then 0-5% ether in hexane in a gradient fashion to yield phenyl 2,4,5-trifluorobenzoate as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951965B2
Source datasetuspto-grants-2015_02
ORD IDord-f126f88ed88749a695d8cc485af23475
Source noteuspto-grants-2015_02