HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349903Erstellt: 25. Oktober 2026
Water → [1-(4-benzyloxybenzyl)-3-phenyl-1H-pyrazol-4-yl]methanol
https://huagongshe.com/reaction/349903
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Edukt | ethyl 1-(4-benzyloxybenzyl)-3-phenyl-1H-pyrazole-4-carboxylate | HCID 23024748 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | [1-(4-benzyloxybenzyl)-3-phenyl-1H-pyrazol-4-yl]methanol | HCID 69420204 | 267,7% |
Reaktionsschritte
Lithium aluminium hydride (884 mg) was added to a solution of ethyl 1-(4-benzyloxybenzyl)-3-phenyl-1H-pyrazole-4-carboxylate (9.61 g) in tetrahydrofuran (50 ml) at 0° C., and the mixture was stirred at 0° C. for one hour. After adding water, the reaction mixture was stirred at room temperature for one hour. After the precipitate was removed by filtration, the filtrate was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and then concentrated. The crystals obtained were collected by filtration to yield [1-(4-benzyloxybenzyl)-3-phenyl-1H-pyrazol-4-yl]methanol (23.10 g, yield: 97%). This was recrystallized from ethyl acetate-hexane. Melting point: 88–89° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07179823B1 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-c289402912204c95b7358d80f6cd0f62 |
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| Quellennotiz | uspto-grants-2007_02 |
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