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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7376Erstellt: 23. Oktober 2026

4-Hydroxybenzaldehyde → 4-Cyclobutoxybenzaldehyde

https://huagongshe.com/de/reaction/7376

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-HydroxybenzaldehydeHCID 126—
EduktCesium carbonateHCID 10796—
EduktSodium HydroxideHCID 14798—
EduktBromocyclobutaneHCID 78110—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-CyclobutoxybenzaldehydeHCID 2198970875,1%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a suspension of 4-hydroxybenzaldehyde (0.12 g) and cesium carbonate (0.49 g) in N,N-dimethylformamide (2 mL) was added cyclobutyl bromide (0.15 g), and the mixture was stirred at 65° C. overnight. To the reaction mixture was added 1 mol/L aqueous sodium hydroxide solution, and the mixture was extracted with diethyl ether. The organic layer was washed with 0.5 mol/L aqueous sodium hydroxide solution, water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give 4-cyclobutyloxybenzaldehyde (0.13 g). To a solution of the obtained 4-cyclobutyloxybenzaldehyde (0.13 g) in methanol (10 mL) was added sodium borohydride (0.056 g), and the mixture was stirred at room temperature overnight. To the reaction mixture was added 1 mol/L hydrochloric acid solution, and the mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to give 4-cyclobutyloxybenzyl alcohol (0.12 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087579B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-97bf7a716be548b498b33e3b8c7e9ac9
Quellennotizuspto-grants-2006_08