1,2-Oxidative Trifluoromethylation of Olefin with Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) and O<sub>2</sub>: Synthesis of α-Trifluoromethyl Ketones

A novel and efficient 1,2-oxidative trifluoromethylation of olefins employing Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) as a trifluoromethyl source is described with O<sub>2</sub> as the oxidant, which provides access to a variety of valuable α-t...

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Main Authors: Shengxue Zhang, Wangchuan Xiao, Jingjing Wu, Fanhong Wu, Houjin Huang, Xiaoyu Ma, Yafei Shi, Chao Liu
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Molecules
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Online Access:https://www.mdpi.com/1420-3049/29/23/5622
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author Shengxue Zhang
Wangchuan Xiao
Jingjing Wu
Fanhong Wu
Houjin Huang
Xiaoyu Ma
Yafei Shi
Chao Liu
author_facet Shengxue Zhang
Wangchuan Xiao
Jingjing Wu
Fanhong Wu
Houjin Huang
Xiaoyu Ma
Yafei Shi
Chao Liu
author_sort Shengxue Zhang
collection DOAJ
description A novel and efficient 1,2-oxidative trifluoromethylation of olefins employing Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) as a trifluoromethyl source is described with O<sub>2</sub> as the oxidant, which provides access to a variety of valuable α-trifluoromethyl-substituted ketones. The broad substrate scope, feasibility of large-scale operation, and derivatization reactions of α-trifluoromethyl ketones demonstrate the promising utility of this protocol.
format Article
id doaj-art-ebf39945ddad4080b7dc368f0f4d5ffb
institution Kabale University
issn 1420-3049
language English
publishDate 2024-11-01
publisher MDPI AG
record_format Article
series Molecules
spelling doaj-art-ebf39945ddad4080b7dc368f0f4d5ffb2024-12-13T16:28:29ZengMDPI AGMolecules1420-30492024-11-012923562210.3390/molecules292356221,2-Oxidative Trifluoromethylation of Olefin with Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) and O<sub>2</sub>: Synthesis of α-Trifluoromethyl KetonesShengxue Zhang0Wangchuan Xiao1Jingjing Wu2Fanhong Wu3Houjin Huang4Xiaoyu Ma5Yafei Shi6Chao Liu7School of Chemical and Environmental Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai 201418, ChinaShanghai-Sanming Engineering Research Center of Green Fluoropharmaceutical Technology, 25 Jingdong Road, Sanming 365004, ChinaSchool of Chemical and Environmental Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai 201418, ChinaSchool of Chemical and Environmental Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai 201418, ChinaSchool of Chemical and Environmental Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai 201418, ChinaSchool of Chemical and Environmental Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai 201418, ChinaSchool of Chemical and Environmental Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai 201418, ChinaSchool of Chemical and Environmental Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai 201418, ChinaA novel and efficient 1,2-oxidative trifluoromethylation of olefins employing Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) as a trifluoromethyl source is described with O<sub>2</sub> as the oxidant, which provides access to a variety of valuable α-trifluoromethyl-substituted ketones. The broad substrate scope, feasibility of large-scale operation, and derivatization reactions of α-trifluoromethyl ketones demonstrate the promising utility of this protocol.https://www.mdpi.com/1420-3049/29/23/5622Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F)trifluoromethylationα-trifluoromethyl ketones
spellingShingle Shengxue Zhang
Wangchuan Xiao
Jingjing Wu
Fanhong Wu
Houjin Huang
Xiaoyu Ma
Yafei Shi
Chao Liu
1,2-Oxidative Trifluoromethylation of Olefin with Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) and O<sub>2</sub>: Synthesis of α-Trifluoromethyl Ketones
Molecules
Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F)
trifluoromethylation
α-trifluoromethyl ketones
title 1,2-Oxidative Trifluoromethylation of Olefin with Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) and O<sub>2</sub>: Synthesis of α-Trifluoromethyl Ketones
title_full 1,2-Oxidative Trifluoromethylation of Olefin with Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) and O<sub>2</sub>: Synthesis of α-Trifluoromethyl Ketones
title_fullStr 1,2-Oxidative Trifluoromethylation of Olefin with Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) and O<sub>2</sub>: Synthesis of α-Trifluoromethyl Ketones
title_full_unstemmed 1,2-Oxidative Trifluoromethylation of Olefin with Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) and O<sub>2</sub>: Synthesis of α-Trifluoromethyl Ketones
title_short 1,2-Oxidative Trifluoromethylation of Olefin with Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F) and O<sub>2</sub>: Synthesis of α-Trifluoromethyl Ketones
title_sort 1 2 oxidative trifluoromethylation of olefin with ag o sub 2 sub ccf sub 2 sub so sub 2 sub f and o sub 2 sub synthesis of α trifluoromethyl ketones
topic Ag(O<sub>2</sub>CCF<sub>2</sub>SO<sub>2</sub>F)
trifluoromethylation
α-trifluoromethyl ketones
url https://www.mdpi.com/1420-3049/29/23/5622
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