Water → N-(2-methoxy-3,4-methylenedioxybenzyl)-N-(p-toluenesulfonyl)aminoacetaldehyde diethylacetal
反応式
[CH2:1]([O:3][CH:4]([O:19][CH2:20][CH3:21])[CH2:5][NH:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]2[O:14][CH2:15][O:16][C:10]=2[C:9]=1[O:17][CH3:18])[CH3:2].C(N(CC)CC)C.[C:29]1([CH3:39])[CH:34]=[CH:33][C:32]([S:35](Cl)(=[O:37])=[O:36])=[CH:31][CH:30]=1.O>C(Cl)Cl>[CH2:20]([O:19][CH:4]([O:3][CH2:1][CH3:2])[CH2:5][N:6]([CH2:7][C:8]1[CH:13]=[CH:12][C:11]2[O:14][CH2:15][O:16][C:10]=2[C:9]=1[O:17][CH3:18])[S:35]([C:32]1[CH:33]=[CH:34][C:29]([CH3:39])=[CH:30][CH:31]=1)(=[O:37])=[O:36])[CH3:21]参加物
実験手順
59.46 g (0.2 mol) of N-(2-methoxy-3,4-methylenedioxybenzyl)aminoacetaldehyde diethylacetal (1) and 28.45 ml (0.204 mol) of triethylamine were dissolved in 100 ml of methylene chloride, to which 38.8 g (0.204 mol) of p-toluenesulfonyl chloride in 80 ml of methylene chloride was added dropwise at 15°-30° C. for 25 minutes. After stirring at room temperature for 30 minutes, 150 ml of water was added to the reaction mixture, which was stirred followed by liquid separation and then being washed with 100 ml of water. After drying the methylene chloride layer over anhydrous magnesium sulfate, the solvent was distilled off under vacuum to obtain 90.3 g of N-(2-methoxy-3,4-methylenedioxybenzyl)-N-(p-toluenesulfonyl)aminoacetaldehyde diethylacetal (2) as an oil. Yield 100%. IR and NMR spectra of the resultant product are listed below. ##STR26##
後処理
- additionwas added dropwise at 15°-30° C. for 25 minutes
- stirringwas stirred
- customfollowed by liquid separation
- washbeing washed with 100 ml of water
- dry with materialAfter drying the methylene chloride layer over anhydrous magnesium sulfate
- distillationthe solvent was distilled off under vacuum
出典と根拠
- ORDレコード
- ord-ee8a19f5cf454e9fa0d76b353b85bded
- 出典データセット
- uspto-grants-1988_09
- 特許番号
- US04769480
反応ノート
読み込み中…