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ChemicalBook CAS DataBase List N,N-Dibenzylacrylamide

N,N-Dibenzylacrylamide synthesis

2synthesis methods
-

Yield:57625-28-2 100%

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine in tetrahydrofuran at -78 - 20; for 1.33333 h;

Steps:

A.6.A

A round bottom flask was charged with tetrahydrofuran (3750 mL) and cooled to-78 C under nitrogen. Acryloyl chloride, (55.7 g, 48. 9mL, 0.615 mol) and diisopropylethylamine (87.3 g, 118 mL, 0.676 mol) were added followed by the slow addition (over a period of 20 minutes) ofdibenzylamine (109.6 g, 106 mL, 0.555 mol). The reaction mixture was allowed to warm up to room temperature and stirred at room temperature for 1.0 hour. A large quantity of white precipitate was observed and thin layer chromatography indicated the reaction was complete. The solids were removed by filtration and the filtrate was concentrated under vacuum to afford a quantitative yield of the title compound.

References:

WO2005/49602,2005,A1 Location in patent:Page/Page column 115; 116