one-pot reductive amination of carbonyl compounds using nabh4 and fe3o4 magnetic nanoparticles

Authors

navabeh nami

mehdi forouzani

hassan ghasemnejad-bosra

omid khalilpour tylami

abstract

one-pot reaction of aldehydes or ketons with aniline derivatives was performed using nabh4 and fe3o4 magnetic nanoparticles (mnps). the optimum amount of fe3o4 mnps was 5 mol% under solvent free condition. the corresponding products were obtained in good to excellent yields. the magnetically recoverable iron oxide nanoparticles are found to be efficient for synthesis of amine derivatives. these nanoparticles are effective in green chemistry and could be successfully reuse. in addition to having the general advantages attributed to the inherent magnetic property of nanocatalyst, fe3o4mnps exhibited exceptionally high catalytic activity compared to other catalysts, to yield the desired products in short reaction time and mild reaction conditions.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

One-pot reductive Amination of Carbonyl Compounds using NaBH4 and Fe3O4 Magnetic Nanoparticles

One-pot reaction of aldehydes or ketons with aniline derivatives was performed using NaBH4 and Fe3O4 magnetic nanoparticles (MNPs). The optimum amount of Fe3O4 MNPs was 5 mol% under solvent free condition. The corresponding products were obtained in good to excellent yields. The magnetically recoverable iron oxide nanoparticles are found to be efficient for synthesis of amine derivatives. These...

full text

One-Pot Facile Synthesis of New 1, 2, 4-‎Triazolidine Derivatives Using Sodium ‎Borohydride and Fe3O4 Magnetic ‎Nanoparticles (MNPs)‎

   One-pot reaction of aldehydes with thiosemicarbazide was performed using NaBH4 and Fe3O4 magnetic nanoparticles (MNPs). The reaction mixture of thiosemicarbazide and carbonyl compounds was stirred under reflux condition in the present of Fe3O4 MNPs and NaBH4.The optimum amount of Fe3O4</su...

full text

One-pot efficient reductive acetylation of aromatic nitro compounds

An efficient one-pot reductive acetylation of aromatic nitro compounds is developed without isolating the intermediate amine. The nitro compound is efficiently reduced by sodium borohydride and catalytic amount of Pd-C in MeOH-water media in presence / absence of alkali, and the amine thus generated is acetylated by acetic anhydride in situ in excellent yields through easy work-up. The techniqu...

full text

Preparation of stable magnetic nanofluids containing Fe3O4@PPy nanoparticles by a novel one-pot route

Stable magnetic nanofluids containing Fe3O4@Polypyrrole (PPy) nanoparticles (NPs) were prepared by using a facile and novel method, in which one-pot route was used. FeCl3·6H2O was applied as the iron source, and the oxidizing agent to produce PPy. Trisodium citrate (Na3cit) was used as the reducing reagent to form Fe3O4 NPs. The as-prepared nanofluid can keep long-term stability. The Fe3O4@PPy ...

full text

Amine dehydrogenases: efficient biocatalysts for the reductive amination of carbonyl compounds

Amines constitute the major targets for the production of a plethora of chemical compounds that have applications in the pharmaceutical, agrochemical and bulk chemical industries. However, the asymmetric synthesis of α-chiral amines with elevated catalytic efficiency and atom economy is still a very challenging synthetic problem. Here, we investigated the biocatalytic reductive amination of car...

full text

A Mild One-Pot Conversion of Alkenes into Amines through Tandem Ozonolysis and Reductive Amination

The selective reduction of hydroperoxyacetals to aldehydes by sodium triacetoxyborohydride provides the basis for a mild one-pot synthesis of amines from alkenes.

full text

My Resources

Save resource for easier access later


Journal title:
iranian chemical communication

Publisher: payame noor university (pnu)

ISSN 2423-4958

volume 3

issue Issue 3, pp. 180-282 2015

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023