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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304001Generated: November 3, 2026

Dimethyl Sulfoxide → Citalopram

https://huagongshe.com/reaction/2304001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactant3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
Reactant1-(4'-Fluorophenyl)-1,3-DihydroIsobenzofuran-5-CarbonitrileHCID 9856159—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductCitalopramHCID 277151.8%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433195B1
Source datasetuspto-grants-2002_08
ORD IDord-7d2f9f407d564c20b06a520bdfdae7cf
Source noteuspto-grants-2002_08