N-formylation of amines using nano cerium oxide as catalyst in inert gas atmosphere

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An eco-friendly N-formylation of amines using nano cerium oxide as a recyclable catalyst under solvent-free and ultrasound irradiation conditions at room temperature

A new method for the synthesis of formamides has been developed by the N-formylation of amines with formic acid in the presence of nano cerium oxide as an efficient and recyclable catalyst under ultrasound irradiation. The reaction system is remarkably simple and environmentally benign.

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Formylation of amines.

Methods to convert amines to formamides are of interest due to the many uses of formamides as synthetic intermediates. These methods include stoichiometric reactions of formylating reagents and catalytic reactions with CO as the carbonyl source. This review discusses the reported stoichiometric and catalytic approaches for preparation of formamides.

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Chemoselective N-tert-butoxycarbonylation and N-formylation of Amines by B(OSO3H)3/SiO2 as an Efficient Heterogeneous and Recyclable Catalyst

A simple, efficient, and cost-effective procedure for the N-tert-butoxycarbonylation and N-formylation of amines (primary, secondary) respectively, with di-tert-butyl dicarbonate and 85% aqueous formic acid under solvent-free condition using B(OSO3H)3/SiO2 (SBSA) as a heterogeneous and recyclable catalyst has been developed. We demonstrated that the resulting catalyst is applicable to various a...

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Synthesis of N-Formylation of Amines using Various Ion Exchanged Forms of Zeolite-A as Catalysts

Formamides represent an important class of intermediates in various organic syntheses. They have been used in the synthesis of some pharmaceutically important compounds such as Fluoroquinolones [1], 1, 2 dihydro quinolones [2] and Nitrogen based heterocyclic compounds [3]. In Lewis bases, its main importance is to catalyze some important reactions such as allylation [4] and hydrosilyation of ca...

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ژورنال

عنوان ژورنال: IOSR Journal of Applied Chemistry

سال: 2017

ISSN: 2278-5736,2278-5736

DOI: 10.9790/5736-1006018690