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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181433Generated: November 2, 2026

2-Fluoro-4-methylaniline → HCID 22025613, compound

https://huagongshe.com/reaction/2181433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-methylanilineHCID 67984—
Reactant2,3,4-Trifluorobenzoic acidHCID 302932—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22025613HCID 22025613—

Reaction Steps

2,3,4-Trifluorobenzoic acid and 2-fluoro-4-methylaniline were reacted in the presence of LiHMDS solution in THF by the general procedure of Example 1, Step B. After workup, 3,4-difluoro-2-[2-fluoro-4-methylanilino]benzoic acid was isolated as a crude pale brown solid which was reacted directly with 2-(aminooxy)ethanol and DMT-MM by the general procedure of Example 6, Step B below, then purified by column chromatography on silica gel (100% EtOAc as eluant) to give 3,4-difluoro-2-(2-fluoro-4-methylanilino)-N-(2-hydroxyethoxy)benzamide as a white solid (44%); m.p. (EtOAc/hexane) 134-139° C. 1H NMR [400 MHz, (CD3)2SO] □ 11.82 (v br s, 1 H), 8.77 (br s, 1 H), 7.41 (ddd, J=8.1, 5.7, 1.6 Hz, 1 H), 7.13-7.00 (m, 2 H), 6.88 (dd, J=8.3, 1.1 Hz, 1 H), 6.82 (ddd, J=8.5, 8.5, 4.2 Hz, 1 H), 4.76 (v br s, 1 H), 3.86 (t, J=5.0 Hz, 2 H), 3.58 (J=5.0 Hz, 2 H), 2.25 (s, 3 H). Anal. calcd. for C16H15F3N2O3: C 56.5; H, 4.4; N, 8.2. Found C, 56.3; H, 4.5; N, 8.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06891066B2
Source datasetuspto-grants-2005_05
ORD IDord-05a9e97d90d64c44b08c981d5c2de822
Source noteuspto-grants-2005_05