反応式
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH2:12])(=[O:11])=[O:10])=[CH:5][CH:4]=1.C(=O)([O-])[OH:14].[NH4+].OO>C(#N)C.O>[O:14]1[CH2:1][CH:2]1[C:3]1[CH:4]=[CH:5][C:6]([S:9]([NH2:12])(=[O:11])=[O:10])=[CH:7][CH:8]=1参加物
5
実験手順
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.
後処理
- additionwere introduced slowly
- customwas consumed
- additionsodium thiosulfate solution (10%, 60 mL) was added slowly
- extractionThe mixture was extracted with dichloromethane (3×80 mL)
- washwashed with brine
- dry with materialdried over magnesium sulfate
- concentrationThe solution was concentrated
出典と根拠
- ORDレコード
- ord-54ff2e7e93da4edfaaa45a41cc0e4417
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06852731B2
関連ノート
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