Reaktion #170231

Reaktionsgleichung

1-Chloroethyl chloroformate

1-benzhydryl-3-((4-chlorothiophen-2-yl)methoxy)-azetidine

Ethanol

→

title compound

Ausbeute 90.9%

3-((4-Chlorothiophen-2-yl)methoxy)-azetidine hydrochloride

Ausbeute 90.9%

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe reaction mixture was stirred overnight
2. 2
   EinengenAfter concentration to dryness
3. 3
   Sonstigethe crude mixture was precipitated from a mixture dichloromethane/diethyl ether

Vorschrift

1-Chloroethyl chloroformate (218 μL, 2.0 mmol) was added to a solution of 1-benzhydryl-3-((4-chlorothiophen-2-yl)methoxy)-azetidine (793 mg, 1.91 mmol) in dichloromethane (10 mL) at 0° C. The reaction mixture was stirred for 1 hour at 0° C. and for an additional 1 hour at room temperature. Ethanol (10 mL) was added and the reaction mixture was stirred overnight. After concentration to dryness, the crude mixture was precipitated from a mixture dichloromethane/diethyl ether to afford the title compound as a white solid (417 mg, 77%) which was used whitout further purification.

Quelle