Tributylstannane → (E)-3-(tributylstannyl)prop-2-en-1-ol
反応式
[CH2:1]([OH:4])[C:2]#[CH:3].[CH2:5]([SnH:9]([CH2:14][CH2:15][CH2:16][CH3:17])[CH2:10][CH2:11][CH2:12][CH3:13])[CH2:6][CH2:7][CH3:8]>C1(C)C=CC=CC=1>[CH2:14]([Sn:9]([CH2:5][CH2:6][CH2:7][CH3:8])([CH2:10][CH2:11][CH2:12][CH3:13])/[CH:3]=[CH:2]/[CH2:1][OH:4])[CH2:15][CH2:16][CH3:17]参加物
4
実験手順
To a mixture of propargyl alcohol (2.24 g) and α,α'-azoisobutyronitrile (0.10 g) in anhydrous toluene (150 ml) is added tributyltin hydride (12.9 ml) and the mixture heated at reflux for about 2.5 hours, cooled and concentrated in vacuo. The crude product is purified by flash chromatography in 15% ether in hexane to give the desired product.
後処理
- temperaturethe mixture heated
- temperatureat reflux for about 2.5 hours
- temperaturecooled
- concentrationconcentrated in vacuo
- customThe crude product is purified by flash chromatography in 15% ether in hexane
出典と根拠
- ORDレコード
- ord-96f7297063ff4536a13820f86abb994a
- 出典データセット
- uspto-grants-1993_06
- 特許番号
- US05216015
反応ノート
読み込み中…