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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17697Erstellt: 23. Oktober 2026

4'-Hydroxyacetophenone → 1-(4-[3-(Diethylamino)propoxy]phenyl)ethanone

https://huagongshe.com/de/reaction/17697

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4'-HydroxyacetophenoneHCID 7469—
EduktPotassium CarbonateHCID 11430—
Edukt3-(Diethylamino)-1-propanolHCID 12159—
EduktMethanesulfonyl chlorideHCID 31297—
EduktMethanesulfonateHCID 85257—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(4-[3-(Diethylamino)propoxy]phenyl)ethanoneHCID 11858361—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a stirred solution of 4′-hydroxyacetophenone (91 mmol) in DMF (80 mL) at rt, solid potassium carbonate (153 mmol) was added. The mesylate prepared from 3-diethylamino-1-propanol and methanesulfonyl chloride (76 mmol) was added to the reaction mixture and heated to 80° C. until completion according to General Procedure Q1, as indicated by TLC or HPLC. After cooling to rt, the reaction mixture was quenched by treating the mixture with saturated sodium bicarbonate. The aqueous layer was poured into EtOAc (100 mL) and washed with H2O (2×50 mL) and brine (50 mL). The organic layer was dried over sodium sulfate, and the solvent was removed in vacuuo to afford the desired 1-{4-[3-(diethylamino)propoxy]phenyl}ethanone. The crude alkylated product was used for further transformation after purifying using silica gel column chromatography (1-4% MeOH/DCM).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737285B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-8310e01060ad4b869e476204a2d27343
Quellennotizuspto-grants-2010_06