Safe and Efficient Reductive Methylation of Primary and Secondary Amines Using N-Methylpyrrolidine Zinc Borohydride
H Alinezhad, M Tajbakhsh, F Salehian…
Index: Alinezhad, Heshmatollah; Tajbakhsh, Mahmood; Salehian, Fatemeh; Fazli, Kazem Synthetic Communications, 2010 , vol. 40, # 16 p. 2415 - 2420
Full Text: HTML
Citation Number: 6
Abstract
An efficient, general procedure for reductive methylation of primary and secondary amines with 37% formaldehyde using N-methylpyrrolidine zinc borohydride (ZBHNMP) as a reducing agent gave the corresponding tertiary amines in excellent yields. The reaction was carried out in tetrahydrofuran under neutral conditions at 0–10° C.
Related Articles:
[Kurosu, Michio; Dey, Sevendu Sekhar; Crick, Dean C. Tetrahedron Letters, 2006 , vol. 47, # 28 p. 4871 - 4875]
[Gonzalez-Galvez, David; Lara, Patricia; Rivada-Wheelaghan, Orestes; Conejero, Salvador; Chaudret, Bruno; Philippot, Karine; Van Leeuwen, Piet W.N.M. Catalysis Science and Technology, 2013 , vol. 3, # 1 p. 99 - 105]
[Caliskan, Hafize; Zaim, Oemer Synthetic Communications, 2010 , vol. 40, # 20 p. 3078 - 3083]
[Zotto, Alessandro Del; Baratta, Walter; Sandri, Mauro; Verardo, Giancarlo; Rigo, Pierluigi European Journal of Inorganic Chemistry, 2004 , # 3 p. 524 - 529]
[Zotto, Alessandro Del; Baratta, Walter; Sandri, Mauro; Verardo, Giancarlo; Rigo, Pierluigi European Journal of Inorganic Chemistry, 2004 , # 3 p. 524 - 529]