Continuous deacylation of amides in a high-temperature and high-pressure microreactor

被引:3
作者
Zou, Pengcheng [1 ]
Wang, Kai [1 ]
Luo, Guangsheng [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, State Key Lab Chem Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
amide deacylation; microreactor; flow hemistry; reaction intensification; ASYMMETRIC HYDROGENATION; ALKALINE-HYDROLYSIS; MECHANISM; CATALYSIS; EXCHANGE; ACID;
D O I
10.1007/s11705-022-2182-y
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The deacylation of amides, which is widely employed in the pharmaceutical industry, is not a fast reaction under normal conditions. To intensify this reaction, a high-temperature and high-pressure continuous microreaction technology was developed, whose space-time yield was 49.4 times that of traditional batch reactions. Using the deacylation of acetanilide as a model reaction, the effects of the temperature, pressure, reaction time, molar ratio of reactants, and water composition on acetanilide conversion were carefully studied. Based on the rapid heating and cooling capabilities, the kinetics of acetanilide deacylation at high temperatures were investigated to determine the orders of reactants and activation energy. This microreaction technology was further applied to a variety of other amides to understand the influence of substituents and steric hindrance on the deacylation reaction.
引用
收藏
页码:1818 / 1825
页数:8
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