HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109918Generated: October 30, 2026
Bromoform → 5-Bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulfonylpyrazole
https://huagongshe.com/reaction/2109918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoform | HCID 5558 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Fipronil sulfone | HCID 3078139 | — |
| Product | 5-Bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulfonylpyrazole | HCID 16727054 | 79% |
Reaction Steps
t-Butylnitrite (84 ml, 0.662 mol) was added to a suspension of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulfonylpyrazole (100 g, 0.221 mol) in bromoform (320 ml). The resulting mixture was heated to 60-70° C. for 3 hours. Another portion of t-butylnitrite (84 ml, 0.662 mol) was added and the mixture stirred at 60-70° C. for a further 2.5 hours. It was then cooled, washed with hexane, hexane-toluene, and then filtered. The solid was washed with pentane and vacuum dried to give 5-bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulfonylpyrazole as a yellow solid (96.69 g, 79% yield), mp 142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07517877B2 |
|---|
| Source dataset | uspto-grants-2009_04 |
|---|
| ORD ID | ord-c3db4804f83c4ebc8a847045eee373b8 |
|---|
| Source note | uspto-grants-2009_04 |
|---|