反応式
[CH2:1](OS(C1C=CC(C)=CC=1)(=O)=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]#[CH:8].[I-:20].[Na+]>CC(C)=O>[I:20][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]#[CH:8]参加物
4
実験手順
A mixture of 7-octynyl-p-toluenesulfonate (18.3 g, 65.2 mmol), sodium iodide (9.77 g, 65.2 mmol) and acetone (91 ml) was allowed to react for four hours under reflux. After cooling, the precipitates were removed by filtration, and the filtrate was concentrated. The resulting residue was purified by silica gel column chromatography (eluent; hexane) to afford 14.5 g of 8-iodo-1-octyne (yield; 94.2%).
後処理
- customto react for four hours
- temperatureunder reflux
- temperatureAfter cooling
- customthe precipitates were removed by filtration
- concentrationthe filtrate was concentrated
- customThe resulting residue was purified by silica gel column chromatography (eluent; hexane)
出典と根拠
- ORDレコード
- ord-15557948ec354671bcc50160cab9f5a5
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06365350B1
関連ノート
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