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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792997Generated: November 2, 2026

Potassium Carbonate → 2-(4-Ethynyl-2-fluoroanilino)-3,4-difluorobenzoic acid

https://huagongshe.com/reaction/1792997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,4-Difluoro-2-[[2-fluoro-4-(trimethylsilylethynyl)phenyl]amino]benzoic acidHCID 22025631—
SolventMethanolHCID 887—
Product2-(4-Ethynyl-2-fluoroanilino)-3,4-difluorobenzoic acidHCID 2202563399%

Reaction Steps

The product of Step B, 3,4-difluoro-2-[[2-fluoro-4-(trimethylsilylethynyl)phenyl]amino]benzoic acid (3.99 g, 11.0 mmol), was dissolved in MeOH (200 mL), to which was added K2CO3 (3.03 g, 22.0 mmol). This mixture was stirred at room temperature for 15 hours, then the reaction solvent removed under reduced pressure. The resulting residue was dissolved in water (50 mL), to which was added 1 M HCl until the pH=4. The resulting pale brown precipitate was collected by filtration and dried to afford the desired product (3.17 g, 99%); m.p. (EtOAc/hexanes) 160–162° C. 1H NMR [400 MHz, (CD3)2SO] δ 13.70 (br s, 1 H), 9.24 (br s, 1 H), 7.82 (ddd, J=9.2, 6.1, 2.1 Hz, 1 H), 7.38 (dd, J=12.0, 1.9, 1 H), 7.21 (ddd, J=8.4, 1.9, 0.8 Hz, 1 H), 7.16 (td, J=9.5, 7.3 Hz, 1 H), 6.96 (ddd, J=8.9, 8.4, 5.4 Hz, 1 H), 4.15 (s, 1 H). Anal. Calcd for C15H8F3NO2: C, 62.4; H, 3.1; N, 4.7. Found: C, 62.4; H, 3.2; N, 4.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078438B2
Source datasetuspto-grants-2006_07
ORD IDord-fc919ded7e0b4f518a6fe0d13ab6a378
Source noteuspto-grants-2006_07