Switchable electrosynthesis of furoquinones in batch and continuous-flow modes

被引:5
|
作者
Yuan, Chengcheng [1 ]
Huang, Xiangxing [1 ]
Qiao, Yaqi [1 ]
Guan, Wenjing [1 ]
Liu, Chengkou [1 ]
Fang, Zheng [1 ]
Li, Yuguang [2 ]
Guo, Kai [1 ,3 ]
机构
[1] Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Peoples R China
[2] Inst Nanjing Adv Biomat & Proc Equipment, Nanjing 211299, Peoples R China
[3] Nanjing Tech Univ, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2023年 / 10卷 / 09期
基金
美国国家科学基金会;
关键词
ORGANIC ELECTROSYNTHESIS; CHEMICAL-CONSTITUENTS; DERIVATIVES; ELECTROCHEMISTRY; NAPABUCASIN; CHEMISTRY; CATALYSIS; OXIDATION;
D O I
10.1039/d3qo00030c
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The directly switchable electrosynthesis of non-deaminated and deaminated furoquinones under catalyst- and oxidant-free conditions was developed. The scale up investigations were carried out in batch and continuous-flow. A dramatic decrease in the yield was obtained, even though only two times more substrate amount was involved compared with the standard conditions in the batch mode. Interestingly, good yields and steady production were achieved using the continuous-flow reactor. Moreover, continuous flow electrosynthesis gave higher production rate under higher current using lesser electrolyte. Higher concentration of substrate was compatible, which contributed to the solvent economy. Therefore, good scalable potential using continuous-flow electrosynthesis reactor was observed.
引用
收藏
页码:2310 / 2317
页数:8
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