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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17651Erstellt: 24. Oktober 2026

4-Hydroxybenzaldehyde → 4-(3-(Diethylamino)propoxy)benzaldehyde

https://huagongshe.com/de/reaction/17651

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-HydroxybenzaldehydeHCID 126—
EduktCesium carbonateHCID 10796—
Edukt3-(Diethylamino)-1-propanolHCID 12159—
EduktMethanesulfonyl chlorideHCID 31297—
EduktMethanesulfonateHCID 85257—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt4-(3-(Diethylamino)propoxy)benzaldehydeHCID 17607043—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a stirred solution of 4-hydroxybenzaldehyde (20 mmol) in DMSO (80 mL) at rt, solid Cs2CO3 (50 mmol) was added. The mesylate prepared from 3-diethylamino-1-propanol and methanesulfonyl chloride, General Procedure P2 (30 mmol) was added to the reaction mixture and heated to 90° C. until the reaction was complete. After cooling to rt, the reaction was quenched by cold H2O (100 mL), and the resulting mixture was extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with brine (3×50 mL) and dried (anhydrous Na2SO4). The solvent was removed in vacuo, and the crude product was purified by silica gel column chromatography (eluting with 10% MeOH in DCM+0.5% Et3N) to afford 4-(3-diethylaminopropoxy)benzaldehyde.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737285B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-db5bf796934549268433edbace0a4a79
Quellennotizuspto-grants-2010_06