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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5901Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/5901

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
PatentnummerUS05246943
Quelldatensatzuspto-grants-1993_09
ORD IDord-27c222d747194cee97fae27c69eb7117
Quellennotizuspto-grants-1993_09