Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 403010Erstellt: 24. Oktober 2026

3,4-Bis(benzyloxy)benzaldehyde → 3,4-Bis(benzyloxy)benzyl alcohol

https://huagongshe.com/de/reaction/403010

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-Bis(benzyloxy)benzaldehydeHCID 79526—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
Produkt3,4-Bis(benzyloxy)benzyl alcoholHCID 7433897,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3,4-Dibenzyloxybenzaldehyde (27) (22.0 mmol) was suspended in 100 mL of anhydrous methanol and cooled to 0° C. under argon. Sodium borohydride (33.0 mmol) was added in portions to the suspension and stirred for 1 h at the same temperature. The resulting solution was then stirred at room temperature overnight. The reaction mixture was evaporated to dryness and the residue was dissolved in ice-water and neutralized with HCl. The solution was then extracted with chloroform and the organic layer was washed successively with water, 10% NaHCO3 solution in water and brine. The organic layer was dried over anhydrous Na2SO4, filtered and evaporated to dryness to provide pure 3,4-Dibenzyloxybenzyl alcohol (28) in 97.5% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08742139B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-17c46815fde54f19a6db355bcab2ae54
Quellennotizuspto-grants-2014_06