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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktAluminium lithium hydrideHCID 21226445—
Eduktethyl 1-(4-benzyloxybenzyl)-3-phenyl-1H-pyrazole-4-carboxylateHCID 23024748—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt[1-(4-benzyloxybenzyl)-3-phenyl-1H-pyrazol-4-yl]methanolHCID 69420204267,7%

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179823B1
Quelldatensatzuspto-grants-2007_02
ORD IDord-c289402912204c95b7358d80f6cd0f62
Quellennotizuspto-grants-2007_02