Solvent-free preparation of amidoalkyl phenols catalyzed by trityl chloride under neutral media-Reference-Cited by-同舟云学术

Solvent-free preparation of amidoalkyl phenols catalyzed by trityl chloride under neutral media

Published:2015-11 Issue:11 Volume:93 Page:1245-1248
ISSN:0008-4042
Container-title:Canadian Journal of Chemistry
language:en
Short-container-title:Can. J. Chem.

Author:

Moosavi-Zare Ahmad Reza¹,Zolfigol Mohammad Ali²,Derakhshan-Panah Fateme²,Daraei Masoume²

Affiliation:

1. Department of Chemistry, Sayyed Jamaleddin Asadabadi University, Asadabad, 6541835583, Iran.

2. Faculty of Chemistry, Bu-Ali Sina University, Hamedan 6517838683, Iran.

Abstract

A one-pot, multicomponent condensation reaction of phenols, aromatic aldehydes, and amides in the presence of catalytic amount of trityl chloride as a homogeneous organocatalyst under solvent-free condition to prepare amidoalkyl phenols has been reported. It is interesting that trityl chloride by in situ generation of trityl carbocation with inherent instability catalyzes the reaction.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Link

http://www.nrcresearchpress.com/doi/pdf/10.1139/cjc-2015-0230

Reference22 articles.

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4. Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature

5. Organocatalyst trityl chloride efficiently promoted the solvent-free synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]-xanthen-11-ones by in situ formation of carbocationic system in neutral media

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