Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Azide | HCID 33558 | — |
| Edukt | 3-(Chloromethyl)-3-methyloxetane | HCID 79112 | — |
| Edukt | Azidooxetane | HCID 22404015 | — |
| Produkt | 3-Azidomethyl-3-methyloxetane | HCID 11147719 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05523424 |
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| Quelldatensatz | uspto-grants-1996_06 |
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| ORD ID | ord-63613d3af50b4ace9d8bd76853e0971a |
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| Quellennotiz | uspto-grants-1996_06 |
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