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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 260081Erstellt: 26. Oktober 2026

Acetone → (2-(Benzyloxy)-3-methoxyphenyl)methanol

https://huagongshe.com/reaction/260081

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
Edukt2-(Benzyloxy)-3-methoxybenzaldehydeHCID 1268087—
EduktSodium borohydrideHCID 4311764—
LösungsmittelEthanolHCID 702—
Produkt(2-(Benzyloxy)-3-methoxyphenyl)methanolHCID 92725086%

Reaktionsschritte

A solution of 43.00 g (0.18 mole) of 2-benzyloxy-3-methoxy-benzaldehyde of Example 1 in 300 mL of absolute ethanol is treated, with stirring, with 7.56 g (0.20 mole) of sodium borohydride. The temperature rises to 50° C. After one-half hour 10 mL of acetone is added, keeping the temperature at less than 60° C. with cooling. After 15 minutes the volatiles are stripped off at reduced pressure. Ice water (500 mL) is added and the product is extracted into 600 mL of ethyl acetate. The dried (NA2SO4) solution is concentrated. The remaining oil is dissolved in 100 mL of warm ether. Petroleum ether is added to turbidity to give 37.70 g (86% yield) of pure product; mp 58°-60° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05525614
Quelldatensatzuspto-grants-1996_06
ORD IDord-f760b7f1e7ff433698dbe74588dcb3ae
Quellennotizuspto-grants-1996_06