Tributylstannane → HCID 12801789、化合物
反応式
[CH2:1]([SnH:5]([CH2:10][CH2:11][CH2:12][CH3:13])[CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4].[F:14][C:15]([C:17]([O:25][Si:26]([CH3:29])([CH3:28])[CH3:27])([CH2:21][CH2:22][CH2:23][CH3:24])[CH2:18][C:19]#[CH:20])=[CH2:16].N(C(C)(C)C#N)=NC(C)(C)C#N>>[F:14][C:15]([C:17]([O:25][Si:26]([CH3:29])([CH3:27])[CH3:28])([CH2:21][CH2:22][CH2:23][CH3:24])[CH2:18]/[CH:19]=[CH:20]/[Sn:5]([CH2:6][CH2:7][CH2:8][CH3:9])([CH2:10][CH2:11][CH2:12][CH3:13])[CH2:1][CH2:2][CH2:3][CH3:4])=[CH2:16]参加物
4
反応条件
- 温度
- 140 °C
実験手順
A mixture of 21.4 ml. of tributylstannane, 18.3 g. of 4-(1'-fluorovinyl)-4-trimethylsilyloxy-1-octyne and azobisisobutyronitrile is heated under an inert atmosphere on an oil bath. Upon reaching 85° C. a rapid exotherm occurs which is moderated to maintain 140° C. using a water bath. After the exotherm the mixture is heated at 135° C. for one hour, then cooled to room temperature. The resulting oil is distilled via a Kugelrohr to give the desired product as 33.68 g. of a light yellow liquid (air bath 160° C., 0.15 mm.).
後処理
- additionA mixture of 21.4 ml
- customUpon reaching 85° C.
- temperatureAfter the exotherm the mixture is heated at 135° C. for one hour
- temperaturecooled to room temperature
- distillationThe resulting oil is distilled via a Kugelrohr
出典と根拠
- ORDレコード
- ord-237f195c789c43c188822207a96e01cd
- 出典データセット
- uspto-grants-1981_10
- 特許番号
- US04297516
反応ノート
読み込み中…