反応 #347805
ord-e4fdaf1f2a6947a299651ebe29481173
反応方程式
反応条件
後処理
- 1その他as described in Preparation 9
- 2その他After 5 days at 20° C. the solvent is removed under reduced pressure
- 3workup.DISSOLUTIONthe residue dissolved
- 4workup.ADDITIONby adding dichloromethane (60 ml) and water (30 ml)
- 5その他After separating the phases the aqueous layer
- 6抽出is extracted with dichloromethane (3×30 ml)
- 7洗浄the combined organic phase washed with saturated aqueous sodium hydrogen carbonate (50 ml)
- 8乾燥The organic phase is dried (MgSO4)
- 9その他the solvent removed under reduced pressure
実験手順
Chloromethyl 4-acryloyloxybutyl carbonate (1.183 g, 5.00 mmol) prepared as described in Preparation 9 is added to a suspension of freeze dried potassium acrylate (0.606 g, 5.50 mmol) and 18-crown-6 (0.066 g, 0.25 mmol) in dimethylformamide (50 ml) under a dry N2 atmosphere. After 5 days at 20° C. the solvent is removed under reduced pressure and the residue dissolved by adding dichloromethane (60 ml) and water (30 ml). After separating the phases the aqueous layer is extracted with dichloromethane (3×30 ml) and the combined organic phase washed with saturated aqueous sodium hydrogen carbonate (50 ml). The organic phase is dried (MgSO4) and the solvent removed under reduced pressure to give 1.24 g (91%) of the title product. 1H NMR (60 MHz, CDCl3): δ 1.82 (4 H, m, CH2 --CH2), 4.23 (4 H, m, 2× CH2 --O), 5.88 (2 H, s, O--CH2 --O), 5.7-6.8 (6 H, 2×CH=CH2).