Sodium Iodide → 6-Phenyl-1-hexyl iodide
反応式
CS(O[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)(=O)=O.[I-:18].[Na+]>CC(C)=O>[C:12]1([CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][I:18])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1参加物
4
実験手順
To 6-phenylhex-1-yl methylsulfonate (4.55 g; 17.3 mmol) dissolved in acetone (100 ml) is added sodium iodide (2.5 g; 173 mmol) and the reaction mixture is heated 2 hours at reflux. The reaction mixture is then concentrated to dryness and partitioned between ether and water. The organic phase is separated, dried, concentrated to dryness and purified with silica chromatography using 10 EtOAc/90 petroleum ether to give 6-phenyl-1-hexyl iodide as a colorless oil which is used directly in Step F.
後処理
- temperaturethe reaction mixture is heated 2 hours
- temperatureat reflux
- concentrationThe reaction mixture is then concentrated to dryness
- custompartitioned between ether and water
- customThe organic phase is separated
- customdried
- concentrationconcentrated to dryness
- custompurified with silica chromatography
出典と根拠
- ORDレコード
- ord-8f17090b939c4349a5cc3b771a243771
- 出典データセット
- uspto-grants-1996_10
- 特許番号
- US05561143
反応ノート
読み込み中…