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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835660Generated: November 1, 2026

2,3,4-Trifluorobenzoic acid → HCID 12135111, compound

https://huagongshe.com/reaction/1835660

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4-Trifluorobenzoic acidHCID 302932—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-amino-3-fluoro-N-methylbenzamideHCID 13249910—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12135111HCID 12135111—

Reaction Steps

2,3,4-Trifluorobenzoic acid and 4-amino-3-fluoro-N-methylbenzamide [Anker et al, Helv. Chim. Acta., 67(3), 706-716 (1984)] were reacted in the presence of LiHMDS solution in THF by the general procedure of Example 1, Step B. After workup, followed by purification by chromatography on silica gel (100% EtOAc as eluant), 3,4-difluoro-2-{2-fluoro-4-[(methylamino)carbonyl]anilino}-benzoic acid was isolated as a pale, yellow-orange solid; m.p. (EtOAc/MeOH) 242-244° C. 1H NMR [400 MHz, (CD3)2SO] δ 13.70 (v br s, 1 H), 9.28 (br s, 1 H), 8.36 (br d, J=4.5 Hz, 1 H), 7.88-7.80 (m, 1 H) 7.69 (dd, J=12.5, 1.7 Hz, 1 H), 7.60 (dd, J=8.5, 1.5 Hz, 1 H), 7.19 (dd, J=16.7, 9.3 Hz, 1 H), 7.01 (ddd, J=8.6, 8.6, 5.8 Hz, 1 H), 2.77 (d, J=4.4 Hz, 3 H). Anal. calcd. for C15H11F3N2O3: C, 55.6; H, 3.4; N, 8.6. Await Found.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770778B2
Source datasetuspto-grants-2004_08
ORD IDord-ca516dea8700407bb94389d81c5cb2d7
Source noteuspto-grants-2004_08