反応式
Cl.C[CH:3](N(C)C)[CH:4]([OH:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.C(NC1C=CC=CC=1)C>[OH-].[Na+]>[C:4]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)(=[O:11])[CH3:3]参加物
5
実験手順
The aqueous layer and the 10% hydrochloric acid washings were joined and the joined solution was mixed with a 10% sodium hydroxide solution (30 ml) to adjust the pH to about 11 and extracted with ethyl acetate (50 ml×3). The extract was washed with a saturated saline solution (50 ml×3), dried and then ethyl acetate was distilled off to obtain a mixture of N-methylephedrine and N-ethylaniline. Yield: 2.4 g (100%). Said two substances can be recovered, separately by distilling the mixture under reduced pressure.
後処理
- extractionextracted with ethyl acetate (50 ml×3)
- washThe extract was washed with a saturated saline solution (50 ml×3)
- customdried
- distillationethyl acetate was distilled off
- customto obtain
- customcan be recovered
- distillationseparately by distilling the mixture under reduced pressure
出典と根拠
- ORDレコード
- ord-688971b6375e4e3099da4d666833e252
- 出典データセット
- uspto-grants-1983_11
- 特許番号
- US04418218
関連ノート
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