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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 259849Erstellt: 25. Oktober 2026

Azide → 3-Azidomethyl-3-methyloxetane

https://huagongshe.com/reaction/259849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzideHCID 33558—
Edukt3-(Chloromethyl)-3-methyloxetaneHCID 79112—
EduktAzidooxetaneHCID 22404015—
Produkt3-Azidomethyl-3-methyloxetaneHCID 1114771997%

Reaktionsschritte

As such, it has been discovered that monofunctional azidooxetane compounds, i.e., 3-azidomethyl-3-R1 -oxetanes, can also be prepared by combining a neat halooxetane with an aqueous metallic azide solution and a phase transfer catalyst (PTC). For example, using the process of the present invention, 3-chloromethyl-3-methyloxetane gives the corresponding 3-azidomethyl-3-methyloxetane (AMMO) in 97% yield. Moreover, 3-bromomethyl-3-hydroxymethyloxetane was previously converted to the corresponding 3-azidomethyl-3-hydroxymethyloxetane in acetone. Using the process of the present invention, however, 3-bromomethyl-3-hydroxymethyloxetane is converted to the corresponding 3-azidomethyl-3-hydroxymethyloxetane, without the use of an organic solvent, using an aqueous sodium azide solution and a phase transfer catalyst. The process of the present invention gives the same result with a faster rate of reaction and without the use of an organic solvent. In addition, 3-chloromethyl-3-methyloxetane 3-chloromethyl-3-phenoxymethyloxetane reacts with an aqueous solution of sodium azide in water with a PTC to give 3-azidomethyl-3-phenoxymethyloxetane in 87% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05523424
Quelldatensatzuspto-grants-1996_06
ORD IDord-63613d3af50b4ace9d8bd76853e0971a
Quellennotizuspto-grants-1996_06