2,6-Dimethylaniline → 2,6-dimethyl-N-prop-2-ynyl-aniline
反応式
[C:1]1(C)[CH:6]=CC(S(OCC#C)(=O)=O)=C[CH:2]=1.[CH3:15][C:16]1[CH:22]=[CH:21][CH:20]=[C:19]([CH3:23])[C:17]=1[NH2:18]>O>[CH3:15][C:16]1[CH:22]=[CH:21][CH:20]=[C:19]([CH3:23])[C:17]=1[NH:18][CH2:6][C:1]#[CH:2]参加物
4
実験手順
Propargyl p-toluenesulphonate (6.0 g, 0.05 mole) was heated with 2,6-dimethylaniline (6.0 g, 0.05 mole) on steam bath for 2 hours, poured into water (100 ml), extracted into methylenedichloride (50 ml), dried (MgSO4), filtered, solvent evaporated and the product distilled to give 2,6-dimethylphenyl propargylamine, identical with that in Route II. Subsequent preparative steps were as outlined in Route II.
後処理
- extractionextracted into methylenedichloride (50 ml)
- dry with materialdried (MgSO4)
- filtrationfiltered
- customsolvent evaporated
- distillationthe product distilled
出典と根拠
- ORDレコード
- ord-617e5ce7239d41e781e7c9ef7186e8dc
- 出典データセット
- uspto-grants-1982_04
- 特許番号
- US04325966
反応ノート
読み込み中…