Synthesis of aryl fluorocyclopropanes from aryl fluorodiazirines and alkenes in continuous flow†

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2024-11-12 DOI:10.1039/d4cc01881h
Hoang-Minh To , Shima Mirakhorli , Thierry Ollevier
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Abstract

Photochemically induced generation of aryl fluorocarbenes from aryl fluorodiazirines and their subsequent [2+1] cycloaddition with alkenes was developed in continuous flow. The in situ generated electrophilic aryl fluorocarbene reacted with a range of alkenes enabling the synthesis of the corresponding 3-fluoro-3-aryl-cyclopropanes in a 5-minute residence time under 380-nm LED irradiation in continuous flow (20 examples). The scaled-up reaction of 3-fluoro-3-(4-chlorophenyl)-3H-diazirine with styrene under irradiation at 380 nm led to the fluorocyclopropane with a 77% yield, providing a throughput yield of 0.945 g h−1.

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用芳基氟二氮杂环烷和烯烃在连续流中合成芳基氟环丙烷。
在连续流中开发了光化学诱导芳基氟二氮杂环丁烷生成芳基氟碳化合物,并随后与烯烃发生 [2+1] 环加成反应。原位生成的亲电芳基氟碳与一系列烯烃反应,在 380-nm LED 连续流照射下,5 分钟停留时间内即可合成相应的 3-氟-3-芳基环丙烷(20 个实例)。在 380 纳米辐照下,3-氟-3-(4-氯苯基)-3H-噻嗪与苯乙烯的放大反应产生了氟环丙烷,收率为 77%,产量为 0.945 克/小时。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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