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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 585345Erstellt: 25. Oktober 2026

Dimethyl Sulfoxide → Citalopram

https://huagongshe.com/reaction/585345

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktSodium hydrideHCID 24758—
Edukt3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
Edukt1-(4'-Fluorophenyl)-1,3-DihydroIsobenzofuran-5-CarbonitrileHCID 9856159—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktCitalopramHCID 277151,8%

Reaktionsschritte

60% Sodium hydride (0.92 g) was dispersed in THF (30 ml). To the obtained suspension was added dropwise a solution of 1-(4′-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile (4.80 g) in THF (10 ml) at 40-50° C. The mixture was stirred at the same temperature for 30 min, and a solution of 3-dimethylaminopropyl chloride (3.2 g) in toluene (20 ml) was added dropwise, which was followed by stirring for 10 min. Then, dimethyl sulfoxide (30 ml) was further added dropwise and the mixture was stirred at 65-70° C. for 3 hr. The reaction mixture was poured into ice water (200 ml) and extracted 3 times with toluene (60 ml). The organic layer was extracted twice with 20% aqueous acetic acid (60 ml). The aqueous layer was neutralized, extracted twice with toluene (60 ml) and washed with water. Anhydrous potassium carbonate (2 g) and silica gel (2 g) were added and the mixture was stirred and filtered. The solvent was evaporated to give 1-(3′-dimethylaminopropyl)-1-(4′-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile (citalopram base) as a viscous oil (3.37 g, 51.6%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06930211B2
Quelldatensatzuspto-grants-2005_08
ORD IDord-c824f135f22a49f3b2845b26f249ac5f
Quellennotizuspto-grants-2005_08