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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
De Gruyter
2014-08-01
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Series: | Green Processing and Synthesis |
Subjects: | |
Online Access: | https://doi.org/10.1515/gps-2014-0043 |