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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898452Generated: November 2, 2026

4-Fluoro-3-(trifluoromethyl)aniline → HCID 178432351, compound

https://huagongshe.com/reaction/1898452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-3-(trifluoromethyl)anilineHCID 75377—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 178496996HCID 178496996—
SolventTolueneHCID 1140—
ProductHCID 178432351HCID 17843235119.4%

Reaction Steps

Under inert atmosphere to a solution of methyl 7-[(2-chloro-6-fluorophenyl)amino]-2-methyl-8H-imidazo[4,5-e][1,3]benzoxazole-4-carboxylate (Step-3 of Intermediate-56, 0.100 g, 0.297 mmol) in dry toluene was added 4-fluoro-3-trifluoromethyl aniline (0.080 g, 0.446 mmol) and trimethyl aluminium (2.0 M solution in toluene) (0.037 g, 0.516 mmol). The reaction mixture was refluxed for 1 h. The reaction mass was quenched in water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate and concentrated. The obtained crude was purified by column chromatography on basic alumina eluting with 0.75-1% DCM: MeOH to afford 0.030 g of the desired product. 1HNMR (DMSO-d6): δ 2.65 (s, 3H), 7.40-7.57 (m, 4H), 7.65 (s, 1H), 8.06 (m, 1H), 8.30 (s, 1H), 9.37 (s, 1H), 10.40 (s, 1H), 11.68 (s, 1H); MS [M+H]+: 522.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519149B2
Source datasetuspto-grants-2013_08
ORD IDord-36c04dde7cb8474da5a1a39b92b94940
Source noteuspto-grants-2013_08