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

Paper ID Volume ID Publish Year Pages File Format Full-Text
41922 45904 2010 9 PDF Available
Title
Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature
Abstract

A highly efficient and simple procedure for the preparation of 1-amidoalkyl-2-naphthols via one-pot three-component condensation reaction of 2-naphthol, arylaldehydes and acetonitrile (Ritter type reaction) in the presence of catalytic amount of trityl chloride at room temperature is described. The reactions proceed in high yields and in relatively short reaction times.

Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (27 K)Download as PowerPoint slideResearch highlights▶ Introducing an efficient new catalyst for synthesis of 1-amidoalkyl-2-naphthols. ▶ The synthesis of bis(1-amidoalkyl-2-naphthol)s. ▶ The use of trityl chloride as a non-acidic organic catalyst. ▶ Performing the reaction at room temperature. ▶ Generality of the method, high yields and short reaction times.

Keywords
Trityl chloride; Organic catalyst; 1-Amidoalkyl-2-naphthol; Multi-component reaction; Ritter type reaction
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Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature
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Publisher
Database: Elsevier - ScienceDirect
Journal: Applied Catalysis A: General - Volume 386, Issues 1–2, 30 September 2010, Pages 179–187
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
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Any Questions? feel free to contact us