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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888673Generated: October 26, 2026

Ethanol → Benzoic acid, 2-fluoro-5-(trifluoromethyl)-, ethyl ester

https://huagongshe.com/reaction/1888673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
Reactant2-Fluoro-5-(trifluoromethyl)benzoyl ChlorideHCID 2734880—
SolventTetrahydrofuranHCID 8028—
ProductBenzoic acid, 2-fluoro-5-(trifluoromethyl)-, ethyl esterHCID 4631138792.3%

Reaction Steps

To a solution of 2-fluoro-5-(trifluoromethyl)benzoyl chloride (5.0 g, 22.0 mmol) in THF (25 mL) was added Et3N (3.1 mL, 22.0 mmol) followed by EtOH (1.3 mL, 22.0 mmol). This mixture was stirred at ambient temperature for 1 h and quenched with saturated, aqueous NH4Cl (10 mL). The layers were separated and the aqueous layer was extracted with 3×10 mL EtOAc and the combined organics were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude material was purified by column chromatography (SiO2, 60% hexanes in EtOAc) to give the title compound (4.8 g, 20.3 mmol, 92% yield). 1H NMR (300 MHz, CDCl3) δ ppm 1.42 (t, J=7.1 Hz, 3 H), 4.43 (q, J=7.1 Hz, 2 H), 7.23-7.34 (m, 1 H), 7.74-7.82 (m, 1 H), 8.23 (dd, J=6.3, 2.4 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501794B2
Source datasetuspto-grants-2013_08
ORD IDord-010d0d3b1849482eb85b651df3a47bf7
Source noteuspto-grants-2013_08