Multigram preparation of 2-alkylpyrimidines in the vapor phase from carboxylic acids and 1,3-diaminopropane over a dual catalyst system

1992 ◽  
Vol 57 (10) ◽  
pp. 2925-2929 ◽  
Author(s):  
John W. Hull ◽  
Kari Otterson
1995 ◽  
Vol 151 (2) ◽  
pp. 323-329 ◽  
Author(s):  
J. Miki ◽  
M. Asanuma ◽  
Y. Tachibana ◽  
T. Shikada

2016 ◽  
Vol 12 ◽  
pp. 1503-1511 ◽  
Author(s):  
Carl J Mallia ◽  
Gary C Walter ◽  
Ian R Baxendale

The flow synthesis of ortho-substituted carboxylic acids, using carbon monoxide gas, has been studied for a number of substrates. The optimised conditions make use of a simple catalyst system compromising of triphenylphosphine as the ligand and palladium acetate as the pre-catalyst. Carbon monoxide was introduced via a reverse “tube-in-tube” flow reactor at elevated pressures to give yields of carboxylated products that are much higher than those obtained under normal batch conditions.


Author(s):  
K. V. Puzitskii ◽  
Ya. T. �idus ◽  
T. F. Bulanova ◽  
K. G. Ryabova ◽  
N. S. Sergeeva

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