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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370317Erstellt: 25. Oktober 2026

Benzyl Alcohol → trans-3-Benzyloxy-4-hydroxytetrahydrofuran

https://huagongshe.com/reaction/370317

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl AlcoholHCID 244—
EduktMagnesium perchlorateHCID 24840—
Edukt3,6-Dioxabicyclo[3.1.0]hexaneHCID 67511—
LösungsmittelIsobutyronitrileHCID 6559—
Produkttrans-3-Benzyloxy-4-hydroxytetrahydrofuranHCID 14307979—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a flask fitted with a condenser and nitrogen inlet was added 3,4-epoxytetrahydrofuran (20 g, 0.23 mol), isobutyronitrile (100 ml, 5 vol), benzyl alcohol (124 g, 1.15 mol, 5 eq.) and finally magnesium perchlorate (10.3 g, 0.046 mol, 0.2 eq). The solution was heated at 100° C. for 24 hours. After cooling to room temperature, the reaction was quenched with water (1000 mL). The phases were separated and the aqueous phase was extracted with ethyl acetate (3×400 mL). After drying the organic phases over MgSO4, filtering and concentrating in vacuo, the trans-3-benzyloxy-4-hydroxytetrahydrofuran was isolated by column chromatography to give 29 g (66% yield) of a clear colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06140516
Quelldatensatzuspto-grants-2000_10
ORD IDord-6b610ebf91754880a244f3c223e634ad
Quellennotizuspto-grants-2000_10