Sodium Iodide → 4-Acetamido-3-iodobenzaldehyde
反応式
[CH:1]([C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10](=[O:12])[CH3:11])=[CH:5][CH:4]=1)=[O:2].FC(F)(F)C([O-])=O.[Tl+3].FC(F)(F)C([O-])=O.FC(F)(F)C([O-])=O.[I-:35].[Na+]>FC(F)(F)C(O)=O.O>[CH:1]([C:3]1[CH:4]=[CH:5][C:6]([NH:9][C:10](=[O:12])[CH3:11])=[C:7]([I:35])[CH:8]=1)=[O:2]参加物
実験手順
To a solution of N-(4-formyl-phenyl)-acetamide (1.25 g, 7.67 mmol) in trifluoroacetic acid (70 mL) was slowly added thallium(III)trifluoroacetate (5.00 g, 9.20 mmol). The reaction mixture was stirred at room temperature for 30 minutes. Then, a solution of sodium iodide (1.19 g, 7.95 mmol) in water (10 mL) was added slowly. The color changed to dark purple and a lot of solid was formed. Stirring continued at room temperature for 16 hours. Solvent was evaporated to half of the volume, and water (50 mL) was added. The pH was adjusted to approximately 13 with 4 N NaOH solution. The mixture was extracted with ethyl acetate (2×100 mL). The organic phase was dried over anhydrous Na2SO4 and concentrated on a rotary evaporator. The solid obtained was washed with ethyl acetate (2×5 mL), ether (2×10 mL), and dried under vacuum to give N-(4-formyl-2-iodo-phenyl)-acetamide as an off-white solid. Yield: 0.760 g (34%).
後処理
- customwas formed
- stirringStirring
- waitcontinued at room temperature for 16 hours
- customSolvent was evaporated to half of the volume, and water (50 mL)
- additionwas added
- extractionThe mixture was extracted with ethyl acetate (2×100 mL)
- dry with materialThe organic phase was dried over anhydrous Na2SO4
- concentrationconcentrated on a rotary evaporator
- customThe solid obtained
- washwas washed with ethyl acetate (2×5 mL), ether (2×10 mL)
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-cf34b0724796436bb6658bfd9bc72a2e
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09238640B2
反応ノート
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