HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 254226Erstellt: 26. Oktober 2026
Water → 5-fluoro-1-methyl-3-trifluoromethyl-1H-pyrazole-4-methanol
https://huagongshe.com/reaction/254226
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 5-fluoro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde | HCID 19754747 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 5-fluoro-1-methyl-3-trifluoromethyl-1H-pyrazole-4-methanol | HCID 17862892 | 95,4% |
Reaktionsschritte
A solution of 36.8 g (187.6 mmoles) of 5-fluoro-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde dissolved in 200 ml of methanol was added, with ice-cooling, into a solution of 3.9 g (102.6 mmoles) of sodium borohydride dissolved in 500 ml of methanol. The mixture was stirred at 0° C. for 30 minutes to give rise to a reaction. After confirmation of the completion of the reaction, the reaction mixture was poured into water and extraction with ethyl acetate was conducted. The resulting organic layer was washed with water and an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to reduced pressure distillation to remove the solvent contained therein, to obtain 35.4 g (yield: 95.4%) of (5-fluoro-1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07875606B2 |
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| Quelldatensatz | uspto-grants-2011_01 |
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| ORD ID | ord-e7fb13350fbb47c9be9b300eae8860b7 |
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| Quellennotiz | uspto-grants-2011_01 |
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