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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 400233Erstellt: 24. Oktober 2026

Oxiranemethanol, 3-[(phenylmethoxy)methyl]- → 3-Allyl-4-(benzyloxy)-3-hydroxy-1-butanol

https://huagongshe.com/de/reaction/400233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxiranemethanol, 3-[(phenylmethoxy)methyl]-HCID 3934498—
EduktHCID 178418473HCID 178418473—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Allyl-4-(benzyloxy)-3-hydroxy-1-butanolHCID 18944106—

Reaktionsbedingungen

Temperatur-40 °C

Reaktionsschritte

A solution of 4-benzyloxy-2,3-epoxy-1-butanol (6.28 g, 32.37 mmol) in anhydrous tetrahydrofuran (75 mL) was added dropwise at -40° C. over a period of 45 minutes, to a 2M solution of allyl magnesium chloride (48.5 mL, 97 mmol) and tetrahydrofuran (50 mL). The solution was stirred at -40° C. for 1 hour, warmed to 0° C. and quenched by addition of aqueous ammonium chloride solution. The tetrahydrofuran layer was separated and the aqueous layer was extracted with ethyl acetate (three times). The combined organic extract was dried (magnesium sulfate), filtered and concentrated to obtain a mixture of compounds A and B.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05827868
Quelldatensatzuspto-grants-1998_10
ORD IDord-757e5a1c8b554ab7918a14250606dd48
Quellennotizuspto-grants-1998_10