HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172097Generated: October 25, 2026
Water → (5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol
https://huagongshe.com/reaction/1172097
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde | HCID 17862886 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol | HCID 17862906 | 106.9% |
Reaction Steps
To a solution of 1.6 g (41.0 mmoles) of sodium borohydride dissolved in 300 ml of methanol was added, with ice-cooling, a solution of 26.5 g (102.5 mmoles) of 5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde dissolved in 200 ml of methanol. The resulting mixture was stirred at 0° C. for 30 minutes 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 28.5 g (yield: 100%) of (5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol.
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-f41b75a68ce9430ba3a31f8d08393a93 |
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| Source note | uspto-grants-2010_11 |
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