Reaktion #346874
ord-c8b12b7d2d594548aeab2c5d3b70d9d0
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturheated to reflux
- 2TemperaturAfter heating for 18 h
- 3Temperaturthe resultant slurry was cooled to room temperature
- 4Filtrationsuction filtered through a short pad of silica gel
- 5WaschenThe solid residue was washed with tetrahydrofuran (2×50 mL)
- 6Einengenconcentrated
- 7workup.DISSOLUTIONThe residue was dissolved in ethyl acetate (2.0 L)
- 8Waschenwashed with water and brine
- 9Trocknenwas dried over MgSO4
- 10FiltrationFiltration and concentration
- 11Sonstigegave a yellow oil which
- 12Sonstigeupon drying
- 13SonstigeThe resultant solid was recrystallized from a mixture of hot ethyl acetate/hexane
Vorschrift
To a stirred mixture of diethyl acetamidomalonate (217 g, 1.0 mol) and 2,3-dibromopropene (240 g, 1.2 mol) in dry tetrahydrofuran (2.50 L), under nitrogen, was added sodium hydride (26.4 g, 1.1 mol) in several portions. The reaction mixture was stirred at room temperature for 30 min, then heated to reflux. After heating for 18 h, the resultant slurry was cooled to room temperature and suction filtered through a short pad of silica gel. The solid residue was washed with tetrahydrofuran (2×50 mL), and the filtrates were combined and concentrated. The residue was dissolved in ethyl acetate (2.0 L), washed with water and brine, and then was dried over MgSO4. Filtration and concentration gave a yellow oil which solidified upon drying. The resultant solid was recrystallized from a mixture of hot ethyl acetate/hexane to give 301 g (89%) of the desired product: m.p. 85°-87° C. 1H NMR (300 MHz, CDCl3) δ1.28 (t, J=7.4 Hz, 6H), 2.04 (s, 3H), 3.57 (s, 2H), 4.27 (m, 4H), 5.55 (bs, 1H), 5.61 (bs, 1H), 6.82 (broad, 1H); IR (KBr) 1745, 1635 cm-1. Anal. Calcd. for C12H18BrNO5 : C, 42.87; H, 5.40; Br, 23.77; N, 4.12. Found: C, 43.25; H, 5.56; Br, 22.97; N, 4.12.