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:22]1([CH3:32])[CH:27]=[CH:26][C:25]([S:28](Cl)(=[O:30])=[O:29])=[CH:24][CH:23]=1.O>C(N(CC)CC)C.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:28]([C:25]1[CH:26]=[CH:27][C:22]([CH3:32])=[CH:23][CH:24]=1)(=[O:30])=[O:29])[CH3:21]参加物
実験手順
N-(2-methoxy-3,4-methylenedioxybenzyl)aminoacetaldehyde diethylacetal (2) in an amount of 59.46 g (0.2 mol) and triethylamine in an amount of 28.45 ml (0.204 mol) were dissolved in 100 ml of methylene chloride, to which 38.88 g (0.204 mol) of p-toluenesulfonyl chloride in 80 ml of methylene chloride was added dropwise at 15°-30° C. over 25 minutes After stirring the mixture at room temperature for 30 minutes, 150 ml of water was added and the reaction mixture was stirred. The methylene chloride layer was separated from the aqueous layer and further washed with 100 ml of water. After drying the methylene chloride layer over anhydrous magnesium sulfate, the solvent was distilled off at reduced pressure to obtain 90.3 g of N-(2-methoxy-3,4-methylenedioxybenzyl)-N-(p-toluenesulfonyl)aminoacetaldehyde diethylacetal (3) as an oil. Yield: 100%. IR and NMR of the resultant product are listed below.
後処理
- additionwas added dropwise at 15°-30° C. over 25 minutes
- stirringthe reaction mixture was stirred
- customThe methylene chloride layer was separated from the aqueous layer
- washfurther washed with 100 ml of water
- dry with materialAfter drying the methylene chloride layer over anhydrous magnesium sulfate
- distillationthe solvent was distilled off at reduced pressure
出典と根拠
- ORDレコード
- ord-65387d2b0b094411a9607cccc19464fa
- 出典データセット
- uspto-grants-1990_10
- 特許番号
- US04963684
反応ノート
読み込み中…