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HERO ID
5973058
Reference Type
Journal Article
Title
Metal free green protocol for the synthesis of bis-spiro piperidine and pyrimidine derivatives
Author(s)
Patil, A; Salunkhe, R
Year
2018
Is Peer Reviewed?
1
Journal
Research on Chemical Intermediates
ISSN:
0922-6168
EISSN:
1568-5675
Volume
44
Issue
5
Page Numbers
3337-3348
DOI
10.1007/s11164-018-3310-7
Web of Science Id
WOS:000429485300025
URL
http://
://WOS:000429485300025
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Abstract
Abstract: A highly efficient one-pot three-component synthesis of bis-spiro piperidine and pyrimidine derivatives has been reported by performing the reaction of formaldehyde, aromatic aniline and 1,3-dicarbonyl compounds. This reaction was carried out at room temperature in 2,2,2-trifluoroethanol (TFE) as a recyclable reaction medium under the metal free condition. The strong hydrogen donor ability and acidic property of TFE plays a key role in accelerating the rate of reaction and initiates the reaction smoothly. The advantageous features of this method are a mild reaction condition, no column chromatographic purification, and high yield of products and recyclability of TFE. Graphical Abstract: [Figure not available: see fulltext.]. © 2018, Springer Science+Business Media B.V., part of Springer Nature.
Keywords
2,2,2-Trifluoroethanol; Bis-spiro piperidine; 1,3-Diaryl-hexahydropyrimidine; Multicomponent reaction; Green synthesis; Reusability
Tags
PFAS
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PFAS Universe
Data Source
Web of Science
2,2,2-Trifluoroethanol
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