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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35283Erstellt: 24. Oktober 2026

Benzyl Bromide → 5-(Benzyloxy)-2-methoxybenzaldehyde

https://huagongshe.com/de/reaction/35283

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktSodium HydroxideHCID 14798—
Edukt5-Hydroxy-2-MethoxybenzaldehydeHCID 358341—
KatalysatorTrioctylmethylammonium chlorideHCID 21218—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(Benzyloxy)-2-methoxybenzaldehydeHCID 1096669491%

Reaktionsschritte

To a stirred suspension of 5-hydroxy-2-methoxybenzaldehyde (306.6 g, prepared by the method of Ulrich et al, J.Org.Chem., 1974, 39, 2437), benzyl bromide (355.8 g) and Adogen 464 (48.5 g) in dichloromethane (600 ml) was added a solution of sodium hydroxide (123.5 g) in water (500 ml). The mixture became warm and the suspension dissolved; additional dichloromethane (300 ml) was added to prevent crystallisation of the benzylated product. After 2 hours, the organic layer was removed, washed twice with water, once with saturated sodium chloride solution, then dried with anhydrous magnesium sulphate. The solution was concentrated, then treated with petroleum spirit to give 5-benzyloxy-2-methoxybenzaldehyde (445.7 g, 91%), m.p. 99°-100°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04766121
Quelldatensatzuspto-grants-1988_08
ORD IDord-09acaa2b0fe944e185cdd2596e974e13
Quellennotizuspto-grants-1988_08