HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232183Generated: October 31, 2026
Bromoform → 5-Bromo-4-nitro-1-(2,3,5,6-tetrafluoro-4-trifluoromethyl-phenyl)-pyrazole
https://huagongshe.com/reaction/2232183
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoform | HCID 5558 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 5-Amino-1-(2,3,5,6-tetrafluoro-4-trifluoromethylphenyl)-4-nitropyrazole | HCID 13933713 | — |
| Product | 5-Bromo-4-nitro-1-(2,3,5,6-tetrafluoro-4-trifluoromethyl-phenyl)-pyrazole | HCID 13933733 | 89.9% |
Reaction Steps
21.6 ml (0.18 mol) of t-butylnitrite are added dropwise to 20.6 g (0.06 mol) of 5-amino-4-nitro-1-(2,3,5,6-tetrafluoro-4-trifluoromethyl-phenyl)-pyrazole in 100 ml (1.125 mol) of bromoform in the course of 10 minutes, while stirring, whereupon the temperature of the reaction mixture rises to 50° C. When the addition has ended, the mixture is stirred at the reflux temperature for a further two hours and is concentrated in vacuo, the residue is taken up in methylene chloride, the mixture is washed several times with saturated sodium bicarbonate solution, 2n-hydrochloric acid and water and dried over sodium sulphate and the solvent is stripped off in vacuo. 22 g (89.9% of theory) of 5-bromo-4-nitro-1-(2,3,5,6-tetrafluoro-4-trifluoromethyl-phenyl)-pyrazole are obtained as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04787930 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-369411d8c0124181964c83686fc0f8d1 |
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| Source note | uspto-grants-1988_11 |
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