HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470785Generated: October 25, 2026
Tetrafluoroboric acid → 4-Fluoro-3-methyl-2-(trifluoromethyl)benzonitrile
https://huagongshe.com/reaction/470785
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | 4-Amino-3-methyl-2-(trifluoromethyl)benzonitrile | HCID 21875210 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Fluoro-3-methyl-2-(trifluoromethyl)benzonitrile | HCID 66624938 | — |
Reaction Steps
4-amino-3-methyl-2-(trifluoromethyl)benzonitrile (CAS 573764-86-0, 2.0 g, 9.99 mmol) was dissolved in fluoroboric acid, HBF4 solution (15 mL) at −10° C. (ice/MeOH). To the pre-cooled solution was added NaNO2, (689 mg, 9.992 mmol) in 2 mL H2O drop by drop under constant stirring. The reaction mixture was allowed to stir for 15 min at −10° C. and filtered off. The white residue was washed with cold EtOH and cold ether to get the diazosalt as a white crystalline solid. The salt is dried over high vacuum for 4-5 h. to provide 1.9 g. The salt was heated up (>250° C.) and sublimed under reduced pressure to get the crude fluoro compound as an oil. The oil is chromatographed to get the pure 4-fluoro-3-methyl-2-(trifluoromethyl)benzonitrile as a clear oil (700 mg): 1H NMR (400 MHz, CDCl3, δ in ppm) 7.68 (dd, J=5.0, 9.0 Hz, 1H), 7.33 (t, J=9 Hz, 1H), 2.43 (quin, J=2 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629167B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-ee0a512a22924060a345e22b960398b3 |
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| Source note | uspto-grants-2014_01 |
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