HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692048Generated: November 1, 2026
Water → 4-Bromo-3-(difluoromethyl)-1-methyl-1H-pyrazole
https://huagongshe.com/reaction/1692048
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(Difluoromethyl)-1-methyl-1H-pyrazole | HCID 54241061 | — |
| Reactant | 5-(difluoromethyl)-1-methyl-1H-pyrazole | HCID 66901778 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-3-(difluoromethyl)-1-methyl-1H-pyrazole | HCID 44249264 | 89% |
Reaction Steps
At from 3 to 5° C., a solution of N-bromosuccinimide (NBS, 54 g, 0.3 mol) in dimethyl-formamide (DMF, 100 ml) was added dropwise to a solution of 3-difluoromethyl-N-methylpyrazole (49.3 g, 0.3 mol; 81.4% pure according to GC analysis) comprising, as minor component, 5.2% of 5-difluoromethyl-N-methylpyrazole, based on the total amount of the isomer mixture, in DMF (100 ml). The reaction mixture was then warmed to room temperature and stirred for a further 12 h. With stirring, the reaction mixture was then poured into water (1000 ml) and extracted twice with methyl tert-butyl ether (MTBE, 300 ml). The organic phases were combined, washed with a saturated aqueous solution of NaCl, dried over magnesium sulfate, filtered and then freed from the solvent under reduced pressure. 4-Bromo-3-difluoromethyl-N-methylpyrazole was obtained as an oil (76.6 g; purity: 74.2% according to GC analysis) comprising 4.5% of unreacted 5-difluoromethyl-N-methylpyrazole. This corresponds to a yield of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153820B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-d2e77615b8c247d3a67974c3b5fbc65d |
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| Source note | uspto-grants-2012_04 |
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