HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172095Generated: October 25, 2026
Water → 4-(Bromomethyl)-5-chloro-1-phenyl-3-(trifluoromethyl)-1H-pyrazole
https://huagongshe.com/reaction/1172095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | (5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol | HCID 17862912 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(Bromomethyl)-5-chloro-1-phenyl-3-(trifluoromethyl)-1H-pyrazole | HCID 17862890 | 279% |
Reaction Steps
A solution of 3.0 g (10.9 mmoles) of (5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol dissolved in 60 ml of diethyl ether was cooled to −10° C. Thereto was added 1.0 g (3.8 mmoles) of phosphorus tribromide. The mixture was stirred at room temperature for 1 hour to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water, followed by extraction with ethyl acetate. The resulting organic layer was washed with an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain 3.6 g (yield: 95.8%) of 4-bromomethyl-5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazole as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833939B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-f8f63eb742ef40ae8a432cc15f93a324 |
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| Source note | uspto-grants-2010_11 |
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