Please use this identifier to cite or link to this item: http://rportal.lib.ntnu.edu.tw:80/handle/77345300/17145
Title: 氨氧化法製備3
Other Titles: Preparation of 3-Cyanopyridine and Benzonitrile by Ammoxidation
Authors: 洪志明
Issue Date: Jun-1983
Publisher: 國立臺灣師範大學研究發展處
Office of Research and Development
Abstract: 3-Cyanopyridine is the intermediate for nicotinamidc and nicotinic acid. Benzonitrile is the intermediate for homosulfamine. A procedure has now been established for the laboratory fluidized-bed ammoxidation of 3-picoline and toluene to form 3-cyanopyridine in 35.2% yield and benzonitrile in 41.5% yield. The effects of reaction temperature, mole ratio of reactants, and amount of catalyst were studied.
URI: http://rportal.lib.ntnu.edu.tw//handle/77345300/17145
Other Identifiers: 4D8F17C7-13B7-14B5-D1C3-D2E5D7BB8C18
Appears in Collections:師大學報

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