Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277132Erstellt: 26. Oktober 2026

Ammonia → 1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylamine

https://huagongshe.com/reaction/277132

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
Edukt1-[Bis(4-chlorophenyl)methyl]azetidin-3-yl methylsulfonateHCID 21896603—
LösungsmittelMethanolHCID 887—
Produkt1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylamineHCID 21896598—

Reaktionsbedingungen

Temperatur-60 °C

Reaktionsschritte

1[Bis(4-chlorophenyl)methyl]azetidin-3-ylamine may be obtained in the following manner:400 cm3 of a mixture of methanol and liquid ammonia (50/50 by volume) are added to 27 g of 1-[bis(4-chlorophenyl)-methyl]azetidin-3-yl methylsulfonate contained in an autoclave previously cooled to around −60° C. The reaction medium is then stirred at 60° C. for 24 hours and then abandoned in the open air in order to allow the evaporation of the ammonia and finally concentrated under reduced pressure (2.7 kPa). The residue is taken up in 500 cm3 of a 0.37 N aqueous sodium hydroxide solution and extracted with four times 500 cm3 of ethyl ether. The combined organic phases are washed successively with twice 100 cm3 of distilled water and 100 cm3 of a saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated under reduced pressure (2.7 kPa). The residue obtained is purified by flash chromatography on silica gel [eluent: dichloromethan/methanol (95/5 by volume)]. 14.2 g of 1-[bis(4-chlorophenyl)methyl]azetidin-3ylamine are obtained in the form of an oil which solidifies into a cream-colored solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06355631B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-6986739e16ed4d9f8879f3b3480cae66
Quellennotizuspto-grants-2002_03