反応式
[CH2:1]([NH2:9])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(N(CC)CC)C.Cl[CH2:18][O:19][CH:20]=[O:21].O>O1CCCC1>[CH3:18][O:19][C:20]([NH:9][CH2:1][CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1)=[O:21]参加物
6
実験手順
To a cold solution consisting of phenethylamine (20g,0.16mol) in tetrahydrofuran (900 mL) was added triethylamine (23 mL, 0.16 mol). To this solution was added dropwise chloromethylformate (64 mL, 0.8 mol). The reaction mixture was then stirred overnight water (450 mL) was added and the layers were separated. The organic layer was washed successively with water (1×200mL) and brine (1×200mL). The organic solvent was dried (anhydrous magnesium sulfate), filtered and concentrated to give the title compound (28 g, 94% yield).
後処理
- additionwas added
- customthe layers were separated
- washThe organic layer was washed successively with water (1×200mL) and brine (1×200mL)
- dry with materialThe organic solvent was dried (anhydrous magnesium sulfate)
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-7ba537965e054dbcaf88d63a2f6e216f
- 出典データセット
- uspto-grants-1997_02
- 特許番号
- US05602145
関連ノート
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