関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Azide | HCID 33557 | — |
| 反応物 | [3-(Bromomethyl)oxetan-3-yl]methanol | HCID 529264 | — |
| 反応物 | 3-Chloromethyl-3-methyloxetane 3-chloromethyl-3-phenoxymethyloxetane | HCID 22404017 | — |
| 反応物 | [3-(Azidomethyl)oxetan-3-yl]methanol | HCID 22404019 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 3-Azidomethyl-3-phenoxymethyloxetane | HCID 22404021 | 87% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05523424 |
|---|
| 出典データセット | uspto-grants-1996_06 |
|---|
| ORD ID | ord-7f3adcefb4774a9fb881adc0618bb4e7 |
|---|
| 出典メモ | uspto-grants-1996_06 |
|---|