反应详情

To 1.03 g (44.8 mmol) of sodium in 50 mL of dry ethanol was added 9.72 g (44.8 mmol) of solid diethyl acetamidomalonate portionwise. This solution was stirred at reflux under nitrogen for 2 h. After cooling to room temperature the solvent was removed under reduced pressure yielding a tan solid. This solid was dried under vacuum about 2 h. The sodium salt of diethyl acetamidomalonate was then suspended in 50 mL of dry toluene and 15.0 g (44.8 mmol) of diethyl 2-(2-bromoethyl)benzylphosphonate in 25 mL of toluene was added dropwise. This solution was stirred at reflux under nitrogen for 36 h. After cooling the solution to room temperature the solid precipitate was removed by filtration and washed with 20 mL of toluene. The combined toluene solutions were concentrated under reduced pressure to yield a viscous oil. This oil was chromatographed on a column of silica gel with ethyl acetate as eluant. The combined fractions were concentrated under pressure to give 7.2 g (34%) of the product as a clear viscous oil. IR(neat): 1745, 1676 (C=O) cm-1. 1H NMR(CDCl3) δ 1.0-6 (m, 12H); 1.8-3.2 (complex m, 9H); 3.7-4.6 (m, 8H); 6.8-7.4 (m, 5). Anal. Calcd. for C22H34NO8P0.5H2O: C, 54.99; H, 7.34; N, 2.92. Found: C, 54.75; H, 7.37; N, 2.97.

1. temperatureat reflux under nitrogen for 2 h
2. customwas removed under reduced pressure
3. customyielding a tan solid
4. customThis solid was dried under vacuum about 2 h
5. stirringThis solution was stirred
6. temperatureat reflux under nitrogen for 36 h
7. temperatureAfter cooling the solution to room temperature the solid precipitate
8. customwas removed by filtration
9. washwashed with 20 mL of toluene
10. concentrationThe combined toluene solutions were concentrated under reduced pressure
11. customto yield a viscous oil
12. customThis oil was chromatographed on a column of silica gel with ethyl acetate as eluant
13. concentrationThe combined fractions were concentrated under pressure