反応式
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N:3]=1.OO.NC(N)=[O:13].C(N)(N)=O.OO.FC(F)(F)C(O)=O.S(S([O-])=O)([O-])=O.[Na+].[Na+].Cl>ClCCl>[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:13]参加物
反応条件
- 温度
- 0 °C
実験手順
Into a mixture of 2-chloro-3-methylpyridine (12.8 g, 100 mmol), urea hydrogen peroxide addition compound ((NH2)2CO.H2O2, 19.8 g, 210 mmol) and dichloromethane (130 ml) was added dropwise anhydrous trifluoroacetic acid (28.2 ml, 200 mmol) at 0° C. under nitrogen flow, and the reaction mixture was stirred at 0° C. for 1 hour. Then, after stirring for 30 minutes and elevating the reaction temperature to room temperature, an aqueous solution (200 ml) of sodium hydrosulfite (20 g) was added, and the reaction mixture was stirred for 15 minutes. 2N hydrochloric acid (50 ml) was added and the mixture was extracted with dichloromethane (120 ml), and after washed with sodium bicarbonate solution, the mixture was dried over magnesium sulfate and the solvent was evaporated, thereby yielding the title compound (9.00 g, 62.7 mmol, 63%) as a pale yellow solid.
後処理
- stirringThen, after stirring for 30 minutes
- customto room temperature
- stirringthe reaction mixture was stirred for 15 minutes
- extractionthe mixture was extracted with dichloromethane (120 ml)
- washafter washed with sodium bicarbonate solution
- dry with materialthe mixture was dried over magnesium sulfate
- customthe solvent was evaporated
出典と根拠
- ORDレコード
- ord-ed9b942820084dbeb4e4a32f7027b488
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07781452B2
関連ノート
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