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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648633Generated: October 30, 2026

Dimethylformamide → 3-(Difluoromethoxy)-2,4,5-trifluorobenzoic acid

https://huagongshe.com/reaction/1648633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantChlorodifluoromethaneHCID 6372—
ReactantSodium HydroxideHCID 14798—
Reactant2,4,5-Trifluoro-3-hydroxybenzoic AcidHCID 2734270—
SolventWaterHCID 962—
Product3-(Difluoromethoxy)-2,4,5-trifluorobenzoic acidHCID 15023781—

Reaction Steps

20 ml of dimethylformamide, followed by 4.97 g (0.026 mole) of 2,4,5-trifluoro-3-hydroxybenzoic acid [(XXIII), X=X'=F], were added in portions, whilst ice-cooling, to a solution of 2.18 g (0.052 mole) of sodium hydroxide in 5 ml of water. Thereafter the solution was stirred for 30 minutes, whilst ice-cooling. The reaction mixture was then transferred to a 200 ml stainless steel autoclave, and 100 ml of dimethylformamide containing 24.0 g (0.277 mole) of chlorodifluoromethane were added to it. The mixture was then stirred at between 100° and 110° C. for 5 hours under pressure. At the end of this time, the reaction mixture was poured into water and extracted with chloroform. The chloroform extracts were washed with water and dried over anhydrous sodium sulfate; the solvent was then removed by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 9:1 by volume mixture of ethyl acetate and ethanol as the eluent, to afford 2.00 g of 3-difluoromethoxy-2,4.5-trifluorobenzoic acid as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436367
Source datasetuspto-grants-1995_07
ORD IDord-5c2ab579aa064597977a1a60988a5586
Source noteuspto-grants-1995_07