Discontinuous two step flow synthesis of m-aminoacetophenone

The continuous flow nitration of acetophenone followed by reduction of the meta isomer has been demonstrated using simple tubular reactors. Because of ease of separation of the desired isomer from the first step, both steps are made continuous, but separately. The continuous flow nitration was carri...

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Bibliographic Details
Main Authors: Tibhe Jagdish, Sharma Yachita, Joshi Ramesh A., Joshi Rohini R., Kulkarni Amol A.
Format: Article
Language:English
Published: De Gruyter 2014-08-01
Series:Green Processing and Synthesis
Subjects:
Online Access:https://doi.org/10.1515/gps-2014-0043