反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][CH2:7][OH:8].C(NC(C)C)(C)C.[CH3:16][O:17][CH2:18][CH2:19][O:20][CH2:21]Cl>ClCCl>[CH3:16][O:17][CH2:18][CH2:19][O:20][CH2:21][O:8][CH2:7][CH2:6][C:2]1[S:1][CH:5]=[CH:4][CH:3]=1参加物
反応条件
- 温度
- 0 °C
実験手順
15.0 g of 2-thiopheneethanol was dissolved in 350 mL of dichloromethane, and 30.2 g of diisopropylamine was added thereto. The resulting mixture was cooled to 0° C. and 17.5 g of 2-methoxyethoxymethyl chloride was added thereto. The resulting mixture was stirred for 2 hours and heated to reflux for 2 hours. The reaction product solution was cooled and concentrated by evaporation under reduced pressure. To the residue, 200 mL of water and 250 mL of n-hexane were added, and the resulting mixture was stirred for 5 minutes. Aqueous layer was discarded, and the organic layer was washed twice with 700 mL portions of water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 21.5 g (yield of 85%) of the title compound as a colorless oil.
後処理
- temperatureheated
- temperatureto reflux for 2 hours
- temperatureThe reaction product solution was cooled
- concentrationconcentrated by evaporation under reduced pressure
- additionTo the residue, 200 mL of water and 250 mL of n-hexane were added
- stirringthe resulting mixture was stirred for 5 minutes
- washthe organic layer was washed twice with 700 mL portions of water
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-e81fb2b8b6d84ee4beb9aff279930772
- 出典データセット
- uspto-grants-2008_11
- 特許番号
- US07449580B2
関連ノート
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