9.
Difference in the rate of reaction in synthesis of 3-substituted
phenyl-1-(3-coumarinyl) propan-1-one derivatives using different
secondary amine catalysts
Nitin
Kumar*, Ankita Bhatnagar, Himanshu Gupta, P.K. Sharma
Department
of Pharmaceutical Technology, MIET. NH-58, Bypass Road, Baghpat
Crossing, Meerut- 250005, U.P., India.
Tel: +91-1212439019, 2439057, Fax: +91-1212439058, Mob:
+91-9990199151, E.mail:
nitinvermakr@gmail.com
Abstract:
The
present study was undertaken to study the effect of different
secondary amines which are used as the dehydrating catalyst in
the Knoevenagel synthetic mechanism for the synthesis of
3-substituted phenyl-1-(3-coumarinyl) propan-1-ones. Various
studies have been done using piperidine as catalyst in the
various condensation reactions. Here in this study differently
arranged secondary amine compounds were used namely: piperidine,
diethylamine and N-isopropylamine, to know their effects on the
reaction pathway especially in the case of reaction time and the
percentage yield of the final products. In the results it was
evaluated that diethylamine has proven to be yielding larger
amounts of final products while the reaction time of piperidine
catalysed reaction was least. N-isopropylamine has proven to be
least effective among two. These observations could further
stimulate the research on the use of other amines apart from
secondary amines as catalyst in condensation recations like
Knoevenagels.
Keywords:
Knoevenagel reaction, piperidine, diethylamine, N-isopropylamine,
coumarin.
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