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2,4-Pentanedione, 3-[(dimethylamino)methylene]- synthesis

3synthesis methods
-

Yield:18856-72-9 87%

Reaction Conditions:

in benzene at 20; for 25 h;Reflux;

Steps:

Synthesis of enaminodiones 5a-i (general procedure).

General procedure: Dimethylformamide dimethyl acetal (15.49 g, 0.13 mol) was added to 1,3-diketone 4 (0.1 mol) in anhydrous benzene (46 mL), the reaction mixture was stirred for 24 h at room temperature and then refluxed for 1 h, using a reflux condenser equipped witha calcium chloride drying tube. Then the solvent and an excess of DMF DMA were removed at reduced pressure, the residue was recrystallized from a proper solvent.

References:

Obydennov;Goncharov;Sosnovskikh, V. Ya. [Russian Chemical Bulletin,2016,vol. 65,# 9,p. 2233 - 2242][Izv. Akad. Nauk, Ser. Khim.,2016,# 9,p. 2233 - 2242]