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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729365Generated: October 31, 2026

Ethanol → Ethyl 2,4,5-trifluoro-3-methylbenzoate

https://huagongshe.com/reaction/729365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
Reactant2,4,5-Trifluoro-3-methylbenzoic acidHCID 11805514—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductEthyl 2,4,5-trifluoro-3-methylbenzoateHCID 2122046177.1%

Reaction Steps

A solution of 3-methyl-2,4,5-trifluorobenzoic acid (Shimizu T., Asai T., Kumai S., Jpn. Kokai Tokkyo Koho (1997) Japanese Appl. JP 95-219069, 4.3 g, 22.6 mmol) in dichloromethane (100 mL) at 0° C. is treated with oxalyl chloride (4.2 g, 33 mmol) followed by N,N-dimethylformamide (2 drops). The mixture is stirred at room temperature for 3 hours, concentrated and dried in vacuo. The acid chloride is diluted with dichloromethane, cooled to 0° C., and treated with absolute ethanol (10 mL, 170 mmol). The resulting solution is stirred at room temperature for 20 hours, poured into saturated NaHCO3 solution and extracted with dichloromethane. The organic extracts are washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to afford the title compound (3.8 g). 1H NMR (200 MHz, CDCl3): δ 7.67-7.26 (m, 1H), 4.44 (q, 2H), 2.27 (dd, 3H), 1.42 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582627B2
Source datasetuspto-grants-2009_09
ORD IDord-7ab4028772ad4a0c9556c22f3dd8e534
Source noteuspto-grants-2009_09