Реакция #1869152
ord-bccd1606f68f46538243c62ad1d15035
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ДругоеThe solvent was removed
- 2workup.ADDITIONthe residue was diluted with 50 mL ethyl acetate
- 3ПромывкаThe solution was washed with saturated aqueous NaHCO3 (50 mL) and brine (50 mL)
- 4Сушкаthe organic phase was dried over MgSO4
- 5Концентрированиеconcentrated
- 6ДругоеThe residue was purified by flash chromatography (hexane/EtOAc 8:1, Rf=0.21)
Методика
The mixture of ethyl 3-oxododecanoate (1.456 g, ca. 5 mmol), ethylene glycol (2.78 mL, 50 mmol) and a catalytic amount of p-TsOH (95 mg, 0.5 mmol) in benzene (50 mL) was heated to 110° C. under an argon atmosphere overnight. The solvent was removed, and the residue was diluted with 50 mL ethyl acetate. The solution was washed with saturated aqueous NaHCO3 (50 mL) and brine (50 mL), and the organic phase was dried over MgSO4 and concentrated. The residue was purified by flash chromatography (hexane/EtOAc 8:1, Rf=0.21) to give ethyl 3,3-ethylenedioxydodecanoate (1.131 g, 3.95 mmol) in 79% overall yield for the above two steps. 1H NMR (500 MHz, CDCl3) δ 0.88 (t, J=7 Hz, 3H), 1.20-1.44 (m, 17H), 1.76-1.82 (m, 2H), 2.65 (s, 2H), 3.94-4.04 (m, 4H), 4.16 (q, J=7 Hz, 2H); 13C NMR (125 MHz, CDCl3) δ 14.1, 22.6, 23.4, 29.22, 29.43, 29.48, 29.62, 31.8, 37.7, 42.5, 60.4, 65.0, 109.4, 169.5.