光催化
比例(比率)
循环(流体动力学)
流量(数学)
流动化学
放大
计算机科学
工艺工程
环境科学
业务
化学
连续流动
生化工程
机械
航空航天工程
工程类
催化作用
物理
有机化学
经典力学
量子力学
作者
Chen‐Guang Liu,Lei Song,Qiong Liu,Weihao Chen,Jinhui Xu,Mu Wang,Bin Zhang,Ting Tan,Zhexuan Lei,Lei Cheng,Saif A. Khan,Jie Wu
标识
DOI:10.1021/acs.oprd.3c00515
摘要
Although continuous flow synthesis using microtubing reactors has provided a wealth of opportunities for homogeneous photochemical synthesis and has proven particularly beneficial in scaling up processes, employing continuous flow technology to scale up heterogeneous photoreactions is challenging due to the issues including handling of solids, poor light penetration, and commonly lengthy reaction time. Here we present a solution to these issues by changing the continuous flow mode to a high-speed circulation flow mode. The high flow rate set in a circulation flow reactor overcomes solid sedimentation to prevent clogging and improve the mixing efficiency. We successfully conducted 100 g-scale C–N and C–S cross-couplings using a heterogeneous photocatalyst and a nickel catalyst in the flow reactor that significantly outperformed conventional batch reactors. The photocatalyst was recycled and reused 10 times to achieve a kilogram-scale synthesis without obvious deactivation. Semicontinuous production was achieved via automated feeding and collection, and a photopromoted gas/liquid/solid three-phase trifluoromethylation reaction was employed. A kilogram-scale amount of starting material was successfully transformed, resulting in a 43.2% yield of trifluridine. Our study suggests that a circulation flow reactor with high flow speed will become a crucial tool in the synthetic chemist's toolbox because of its simple infrastructure, ease of operation and automation, significant efficiency improvement compared to conventional batch reactors, scalability, improved safety, and tolerance of solids.
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