Synthesis of CF<sub>3</sub>CH<sub>2</sub>‐Amides/Propiolamides/Acrylamides: The TfOH Catalyzed Reactions of Nitrile Compounds with CF<sub>3</sub>CHN<sub>2</sub>

Abstract An efficient and operationally simple protocol to access N ‐(2,2,2‐trifluoroethyl)amides/propiolamides and acrylamides via direct conversion of easily accessible nitriles (aryl/alkyl/alkynyl/vinyl) and in situ generated CF 3 CHN 2 as trifluoroethylating reagent has been developed. The protocol offers broad functional group tolerance under mild reaction conditions. Furthermore, the conversion of trifluoroethylated propiolamide into its triazole analog via Ru‐catalyzed [3+2] cycloadditions using BnN 3 clearly indicates its versatility in the synthetic applications.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2024-10-14
DOI
https://doi.org/10.1002/adsc.202401120
Primary Topic
Organic and Inorganic Chemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of CF3CH2‐Amides/Propiolamides/Acrylamides: The TfOH Catalyzed Reactions of Nitrile Compounds with CF3CHN2

Avijit Goswami, Madan Kumar, Manisha Lamba, Soni Devi
Advanced Synthesis & Catalysis
Organic and Inorganic Chemical Reactions
article

Synthesis of CF3CH2‐Amides/Propiolamides/Acrylamides: The TfOH Catalyzed Reactions of Nitrile Compounds with CF3CHN2

Avijit Goswami, Madan Kumar, Manisha Lamba, Soni Devi
article en

Abstract

Abstract An efficient and operationally simple protocol to access N ‐(2,2,2‐trifluoroethyl)amides/propiolamides and acrylamides via direct conversion of easily accessible nitriles (aryl/alkyl/alkynyl/vinyl) and in situ generated CF 3 CHN 2 as trifluoroethylating reagent has been developed. The protocol offers broad functional group tolerance under mild reaction conditions. Furthermore, the conversion of trifluoroethylated propiolamide into its triazole analog via Ru‐catalyzed [3+2] cycloadditions using BnN 3 clearly indicates its versatility in the synthetic applications.

Advanced Synthesis & CatalysisVol. 367(1)
Indian Institute of Technology Ropar (IN)
Indian Institute of Technology Ropar
Openalex Percentile: Top 86%
Organic and Inorganic Chemical Reactions
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