Derivatives of Cardanol through the Ene Reaction with Diethyl Azodicarboxylate
AUTOR(ES)
Biswas, Atanu, Alves, Carlucio R., Trevisan, Maria T. S., Berfield, Janet, Furtado, Roselayne F., Liu, Zengshe, Cheng, Huai N.
FONTE
J. Braz. Chem. Soc.
DATA DE PUBLICAÇÃO
2016-06
RESUMO
Cardanol is an alkyl/alkenyl phenolic material obtained from cashew nut shell liquid (CNSL), which is a byproduct of cashew nut processing. In an effort to develop new uses, cardanol was derivatized for the first time with diethyl azodicarboxylate (DEAD) through the ene reaction. The reaction was facile and required only the application of heat without a catalyst. Both conventional heating and microwave heating were shown to be effective; the latter entailed much shorter reaction time and substantial energy savings. The reaction product (a hydrazino-ester derivative of cardanol) was characterized by nuclear magnetic resonance (NMR). The product increased in viscosity with time and may be useful as a viscosifier in oil-based commercial formulations and as a synthon for further organic reactions.
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