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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluoro-3-(trifluoromethyl)aniline | HCID 75377 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 178496996 | HCID 178496996 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178432351 | HCID 178432351 | 19.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519149B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-36c04dde7cb8474da5a1a39b92b94940 |
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| Source note | uspto-grants-2013_08 |
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