反応式
Br.[CH2:2]([NH:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[C:15]([O:21][CH3:22])[CH:14]=1)[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[OH-].[Na+]>O>[CH2:2]([NH:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[C:15]([O:21][CH3:22])[CH:14]=1)[CH2:3][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1参加物
4
反応条件
- 温度
- 0 °C
実験手順
25 g of the latter hydrobromide were dissolved in 250 ml of hot water and the solution was cooled to 0° C. and made alkaline with 40 ml of 2 N sodium hydroxide. The mixture was extracted 3 times with 100 ml of ethyl acetate and the organic extracts were washed with water until the wash water had a pH of 7 to 8. The extracts were dried over sodium sulfate, were filtered and evaporated to dryness under reduced pressure to obtain 19 g of N-phenethyl-3,4-dimethoxyphenethylamine.
後処理
- extractionThe mixture was extracted 3 times with 100 ml of ethyl acetate
- washthe organic extracts were washed with water until the wash water
- dry with materialThe extracts were dried over sodium sulfate
- filtrationwere filtered
- customevaporated to dryness under reduced pressure
出典と根拠
- ORDレコード
- ord-667f98f9fa514bd293cae9b10b6fc01d
- 出典データセット
- uspto-grants-1979_11
- 特許番号
- US04175136
関連ノート
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