Issue 2, 2012

(±)-Camphor-10-sulfonic acid catalyzed direct one-pot three-component Mannich type reaction of alkyl (hetero)aryl ketones under solvent-free conditions: application to the synthesis of aminochromans

Abstract

Direct three-component Mannich type reactions of (hetero)aromatic ketones with aromatic aldehydes and aromatic amines were efficiently catalyzed by camphor-10-sulfonic acid at ambient temperature under solvent free conditions to afford β-amino ketones in good to excellent yields. Syntheses of aminochromans were accomplished from one of the Mannich adducts via an unprecedented route involving intramolecular etherification with CuI/8-hydroxyquinoline.

Graphical abstract: (±)-Camphor-10-sulfonic acid catalyzed direct one-pot three-component Mannich type reaction of alkyl (hetero)aryl ketones under solvent-free conditions: application to the synthesis of aminochromans

Supplementary files

Article information

Article type
Paper
Submitted
30 Aug 2011
Accepted
27 Sep 2011
First published
10 Nov 2011

RSC Adv., 2012,2, 480-486

(±)-Camphor-10-sulfonic acid catalyzed direct one-pot three-component Mannich type reaction of alkyl (hetero)aryl ketones under solvent-free conditions: application to the synthesis of aminochromans

K. Kundu and S. K. Nayak, RSC Adv., 2012, 2, 480 DOI: 10.1039/C1RA00652E

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