Literature DB >> 29320204

Dehydration of Amides to Nitriles under Conditions of a Catalytic Appel Reaction.

Sergei A Shipilovskikh1, Vladimir Yu Vaganov1, Elena I Denisova1, Aleksandr E Rubtsov1, Andrei V Malkov2,3.   

Abstract

A highly expedient protocol for a catalytic Appel-type dehydration of amides to nitriles has been developed that employs oxalyl chloride and triethylamine along with triphenylphosphine oxide as a catalyst. The reactions are usually complete in less than 10 min with only a 1 mol % catalyst loading. The reaction scope includes aromatic, heteroaromatic, and aliphatic amides, including derivatives of α-hydroxy and α-amino acids.

Entities:  

Year:  2018        PMID: 29320204     DOI: 10.1021/acs.orglett.7b03862

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  An Entry to Enantioenriched 3,3-Disubstituted Phthalides through Asymmetric Phase-Transfer-Catalyzed γ-Alkylation.

Authors:  Marina Sicignano; Rosaria Schettini; Giovanni Pierri; Maria Leda Marino; Irene Izzo; Francesco De Riccardis; Luca Bernardi; Giorgio Della Sala
Journal:  J Org Chem       Date:  2020-05-27       Impact factor: 4.354

2.  A trustworthy mechanochemical route to isocyanides.

Authors:  Francesco Basoccu; Federico Cuccu; Federico Casti; Rita Mocci; Claudia Fattuoni; Andrea Porcheddu
Journal:  Beilstein J Org Chem       Date:  2022-06-22       Impact factor: 2.544

3.  Development and Utilization of a Palladium-Catalyzed Dehydration of Primary Amides To Form Nitriles.

Authors:  Mohammed H Al-Huniti; José Rivera-Chávez; Katsuya L Colón; Jarrod L Stanley; Joanna E Burdette; Cedric J Pearce; Nicholas H Oberlies; Mitchell P Croatt
Journal:  Org Lett       Date:  2018-09-17       Impact factor: 6.005

  3 in total

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