反応式
[CH2:1]([O:3][CH2:4][CH2:5][OH:6])[CH3:2].[H-].[Na+].I[CH2:10][C:11]([OH:13])=[O:12]>CN(C=O)C>[CH2:1]([O:3][CH2:4][CH2:5][O:6][CH2:10][C:11]([OH:13])=[O:12])[CH3:2]参加物
5
実験手順
2-Ethoxyethanol (0.88 mL, 11 mmol) and sodium hydride (60% in oil, 1.08 g, 27 mmol) were stirred in DMF (20 mL) for 5 min. Iodoacetic acid (2.02 g, 10.9 mmol) was dissolved in DMF (20 mL) and added dropwise to the suspension. The thick orange suspension was stirred at rt for 3 hours. The reaction was quenched by slowly adding water (10 mL), followed by hydrochloric acid (4 M, 5 mL). The reaction mixture was extracted with dichloromethane (3×50 mL) and the combined organic layers dried over sodium sulfate, filtered and evaporated yielding a clear oil. The residue was purified by distillation under reduced pressure to give the product (1.1 g, 68%) as an oil.
後処理
- additionadded dropwise to the suspension
- customThe reaction was quenched by slowly adding water (10 mL)
- extractionThe reaction mixture was extracted with dichloromethane (3×50 mL)
- dry with materialthe combined organic layers dried over sodium sulfate
- filtrationfiltered
- customevaporated
- customyielding a clear oil
- distillationThe residue was purified by distillation under reduced pressure
出典と根拠
- ORDレコード
- ord-1e8bfc91fc1542729e69fa047884cd2f
- 出典データセット
- uspto-grants-2007_09
- 特許番号
- US07268232B2
関連ノート
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