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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181470Generated: October 26, 2026

2,3,4-Trifluorobenzoic acid → 3,4-Difluoro-2-[[2-fluoro-4-(methylthio)phenyl]amino]benzoic acid

https://huagongshe.com/reaction/2181470

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4-Trifluorobenzoic acidHCID 302932—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-Fluoro-4-(methylsulfanyl)anilineHCID 22025617—
SolventTetrahydrofuranHCID 8028—
Product3,4-Difluoro-2-[[2-fluoro-4-(methylthio)phenyl]amino]benzoic acidHCID 2202569452%

Reaction Steps

2,3,4-Trifluorobenzoic acid and the product of Example 26, Step B, 2-fluoro-4-methylthioaniline, were reacted in the presence of LiHMDS solution in THF by the general procedure of Example 1, Step B. After workup, this material was purified by dry flash column chromatography on silica (0.5% Et2O in 1:1 CH2Cl2/hexanes as eluant) to afford 3,4-difluoro-2-[[2-fluoro-4-(methylthio)phenyl]amino]benzoic acid as a cream solid (52%); m.p. (Et2O/hexanes) 210-220° C. 1H NMR (400 MHz, CDCl3) δ 13.70 (br s, 1 H), 9.24 (br s, 1 H), 7.81 (ddd, J=9.0, 6.1, 2.1 Hz, 1 H), 7.20 (dd, J=11.8, 1.9 Hz, 1 H), 7.03-6.99 (m, 3 H), 2.47 (s, 3 H). Anal. Calcd for C14H10F3NO2S-0.125 Et2O: C, 54.0; H, 3.5; N, 4.3. Found: C, 54.2; H, 3.3; N, 4.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06891066B2
Source datasetuspto-grants-2005_05
ORD IDord-1f40a34939f44ecda7c50426c7674ee9
Source noteuspto-grants-2005_05