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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181465Generated: November 2, 2026

2,3,4-Trifluorobenzoic acid → HCID 12135109, compound

https://huagongshe.com/reaction/2181465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4-Trifluorobenzoic acidHCID 302932—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 22025687HCID 22025687—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12135109HCID 12135109—

Reaction Steps

2,3,4-Trifluorobenzoic acid and the product of Example 25, Step A, 2-fluoro-4-(3-methoxy-1-propynyl)aniline, 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 (10% EtOAc/hexanes as eluant), 3,4-difluoro-2-[[2-fluoro-4-(3-methoxy-1-propynyl)phenyl]amino]-benzoic acid was isolated (62%) as a pale yellow solid; m.p. (EtOAc/hexanes) 221-223° C. 1H NMR [400 MHz, (CD3)2SO] δ 13.60 (br s, 1 H), 9.27 (br s, 1 H), 7.85-7.79 (m, 1H,), 7.36 (dd, J=12.0, 1.8 Hz, 1 H), 7.20 (dd, J=8.3, 1.5 Hz, 1 H), 7.18-7.11 (m, 1 H), 6.96 (td, 8.8, 5.5 Hz, 1 H), 4.31 (s, 2 H), 3.32 (s, 3H ). Anal. Calcd for C17H12F3NO3: C, 60.9; H, 3.6; N, 4.2. Found: C, 61.4; H, 3.6; N, 4.2. Step C: Preparation of 3,4-difluoro-2-[[2-fluoro-4-(3-methoxypropyl)phenyl]-amino]benzoic acid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06891066B2
Source datasetuspto-grants-2005_05
ORD IDord-fd535465446845438f29357f2fbeab10
Source noteuspto-grants-2005_05