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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10272Generated: October 26, 2026

Ethanol → Benzoic acid, 2,4,5-trifluoro-, ethyl ester

https://huagongshe.com/reaction/10272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantOxalyl chlorideHCID 65578—
Reactant2,4,5-Trifluorobenzoic acidHCID 521170—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductBenzoic acid, 2,4,5-trifluoro-, ethyl esterHCID 277439797.3%

Reaction Steps

To a solution of 2,4,5-trifluorobenzoic acid (10.85 g, 61.6 mmol) in dichloromethane (100 mL) is added oxalyl chloride (13.5 mL, 154 mmol) and N,N-dimethylformamide (1 drop). After 45 minutes, the reaction mixture is concentrated under vacuum. The resulting residue is dissolved in dichloromethane (100 mL), and to this solution is added ethanol (18 mL, 310 mmol). After 30 minutes, the reaction mixture is diluted with dichloromethane and washed with saturated NaHCO3, water, and brine. The organic layer is dried over MgSO4, filtered, and the filtrate is concentrated to afford the title compound as an oil (12.23 g). 1H NMR(CDCl3): δ 7.85–7.73 (m, 1H), 7.06–6.94 (m, 1H), 4.38 (q, 2H), 1.38 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094780B1
Source datasetuspto-grants-2006_08
ORD IDord-3877a34e25a14eca872308956d9ca54b
Source noteuspto-grants-2006_08