Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10274Generated: October 25, 2026

Ethanol → Benzoic acid, 2,3,4-trifluoro-, ethyl ester

https://huagongshe.com/reaction/10274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantOxalyl chlorideHCID 65578—
Reactant2,3,4-Trifluorobenzoic acidHCID 302932—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductBenzoic acid, 2,3,4-trifluoro-, ethyl esterHCID 59455997.3%

Reaction Steps

To a solution of 2,3,4-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 (3 drops). 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 7.93–7.67 (m, 1H), 7.09–6.96 (m, 1H), 4.39 (q, 2H), 1.40 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094780B1
Source datasetuspto-grants-2006_08
ORD IDord-1ce2e721306346368ed59e7d64aa7c46
Source noteuspto-grants-2006_08