反応式
[CH2:1]([C:13]1[S:14][CH:15]=[CH:16][CH:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[Li]CCCC.[CH3:23][Sn:24](Cl)([CH3:26])[CH3:25]>C1COCC1>[CH2:1]([C:13]1[S:14][C:15]([Sn:24]([CH3:26])([CH3:25])[CH3:23])=[CH:16][CH:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]参加物
反応条件
- 温度
- -78 °C
実験手順
A solution of 2-dodecylthiophene (5.18 g, 20.5 mmol) in dry THF (90 mL) was cooled to −78° C., and a solution of n-BuLi (2.5 M, 12.3 mL, 30.8 mmol) was then added slowly. This mixture was stirred at −78° C. for additiona 10 minutes, and then allowed to warm to room temperature and stirred at room temperature for 30 minutes, before it was cooled back to −78° C. A solution of trimethylstannyl chloride (1.0 M, 31 mL, 31.0 mmol) was added slowly. This mixture was stirred at −78° C. for 2 hours, and then allowed to warm to room temperature, and stirred at room temperature overnight. The reaction was quenched by water (20 mL), and the reaction mixture was diluted with hexane (200 mL), washed with water, dried over Na2SO4, and concentrated on a rotary evaporator, leading to a slightly yellow oil (8.35 g, 98.0%), which was directly used in the next step without further purification.
後処理
- temperatureto warm to room temperature
- stirringstirred at room temperature for 30 minutes, before it
- temperaturewas cooled back to −78° C
- stirringThis mixture was stirred at −78° C. for 2 hours
- temperatureto warm to room temperature
- stirringstirred at room temperature overnight
- customThe reaction was quenched by water (20 mL)
- additionthe reaction mixture was diluted with hexane (200 mL)
- washwashed with water
- dry with materialdried over Na2SO4
- concentrationconcentrated on a rotary evaporator
- customwas directly used in the next step without further purification
出典と根拠
- ORDレコード
- ord-fc08016ac65742edad441d6d978091f4
- 出典データセット
- uspto-grants-2013_12
- 特許番号
- US08598575B2
関連ノート
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