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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878756Generated: October 31, 2026

Ethanol → Ethyl 3-fluoro-4-(trifluoromethoxy)benzoate

https://huagongshe.com/reaction/878756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Fluoro-4-(trifluoromethoxy)benzoic acidHCID 2783356—
ProductEthyl 3-fluoro-4-(trifluoromethoxy)benzoateHCID 6828942264%

Reaction Steps

To a solution of 3-fluoro-4-(trifluoromethoxy)benzoic acid (1.00 g, 4.46 mmol) in ethanol (10 ml) was added thionyl chloride (1.33 g, 11.2 mmol) at 0° C. The reaction solution was slowly warmed to room temperature, and stirred at the same temperature overnight. The reaction solution was poured into saturated aqueous sodium bicarbonate solution, and extracted with ethyl acetate twice. The organic layer was combined, washed with saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:0→9:1) to give ethyl 3-fluoro-4-(trifluoromethoxy)benzoate (0.72 g, 64%) as a colorless and clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987445B2
Source datasetuspto-grants-2015_03
ORD IDord-691dfc1024ad4153a62788f5fe246dd1
Source noteuspto-grants-2015_03