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Hydrogen Peroxide → 4-(Oxiran-2-yl)benzene-1-sulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Peroxide | HCID 784 | — |
| 反応物 | Ammonium Bicarbonate | HCID 14013 | — |
| 反応物 | 4-(Sulfonamido)styrene | HCID 280935 | — |
| 溶媒 | Acetonitrile--water (1/1) | HCID 18373917 | — |
| 生成物 | 4-(Oxiran-2-yl)benzene-1-sulfonamide | HCID 22574283 | 26,100.9% |
反応手順
To a suspension of 4-sulfonamidostyrene (1.83 g, 0.01 mmol) and ammonium hydrogencarbonate (1.6 g, 0.02 mol) in acetonitrile/water (60 mL/30 mL) was added hydrogen peroxide (30% solution, 10 mL, 0.09). The mixture was kept in dark without stirring for 72 hours during which two portion of hydrogen peroxide (5 mL each) were introduced slowly. While HPLC showed all of the starting 4-sulfonamidostyrene was consumed, sodium thiosulfate solution (10%, 60 mL) was added slowly and stirred for 15 minutes. The mixture was extracted with dichloromethane (3×80 mL). The organic phases were combined, washed with brine and dried over magnesium sulfate. The solution was concentrated to give the crude title compound (0.52 g) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06852731B2 |
| 出典データセット | uspto-grants-2005_02 |
| ORD ID | ord-54ff2e7e93da4edfaaa45a41cc0e4417 |
| 出典メモ | uspto-grants-2005_02 |