GRINDING SYNTHESIS OF 2-AMINO-4H-CHROMENES USING 3,3-(BUTANE-1,4-DIYL) BIS (1,2-DIMETHYL- 1H-IMIDAZOLE-3-IUM)Br-CAN AS A NOVEL REAGENT

A clean and environmentally benign route to 2-amino-4H-chromenes has been developed via three-component condensation reaction of various benzyl alcohols, malononitrile and 1-naphthol, using a catalytical amount of CAN and a reusable ionic liquid 3,3-(Butane-1,4-diyl)bis(1,2-dimethyl-1H-imidazole-3-i...

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Autores principales: NIKPASSAND,MOHAMMAD, FEKRI,LEILA ZARE, AHMADI,PARVIN
Lenguaje:English
Publicado: Sociedad Chilena de Química 2017
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072017000100019
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spelling oai:scielo:S0717-970720170001000192017-05-05GRINDING SYNTHESIS OF 2-AMINO-4H-CHROMENES USING 3,3-(BUTANE-1,4-DIYL) BIS (1,2-DIMETHYL- 1H-IMIDAZOLE-3-IUM)Br-CAN AS A NOVEL REAGENTNIKPASSAND,MOHAMMADFEKRI,LEILA ZAREAHMADI,PARVIN Chromenes Benzyl alcohols Ionic Liquid Multicomponent reaction 1-Naphthol Malononitrile A clean and environmentally benign route to 2-amino-4H-chromenes has been developed via three-component condensation reaction of various benzyl alcohols, malononitrile and 1-naphthol, using a catalytical amount of CAN and a reusable ionic liquid 3,3-(Butane-1,4-diyl)bis(1,2-dimethyl-1H-imidazole-3-ium) bromide ([BDBDMIm]Br) as a catalyst at room temperature. The present methodology offers several advantages such as solvent-free conditions, excellent yields, simple procedure, mild conditions and reduced environmental consequences. The ionic liquid was recovered and reused. All of synthesized compounds were characterized by IR, NMR and elemental analyses.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.62 n.1 20172017-03-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072017000100019en10.4067/S0717-97072017000100019
institution Scielo Chile
collection Scielo Chile
language English
topic Chromenes
Benzyl alcohols
Ionic Liquid
Multicomponent reaction
1-Naphthol
Malononitrile
spellingShingle Chromenes
Benzyl alcohols
Ionic Liquid
Multicomponent reaction
1-Naphthol
Malononitrile
NIKPASSAND,MOHAMMAD
FEKRI,LEILA ZARE
AHMADI,PARVIN
GRINDING SYNTHESIS OF 2-AMINO-4H-CHROMENES USING 3,3-(BUTANE-1,4-DIYL) BIS (1,2-DIMETHYL- 1H-IMIDAZOLE-3-IUM)Br-CAN AS A NOVEL REAGENT
description A clean and environmentally benign route to 2-amino-4H-chromenes has been developed via three-component condensation reaction of various benzyl alcohols, malononitrile and 1-naphthol, using a catalytical amount of CAN and a reusable ionic liquid 3,3-(Butane-1,4-diyl)bis(1,2-dimethyl-1H-imidazole-3-ium) bromide ([BDBDMIm]Br) as a catalyst at room temperature. The present methodology offers several advantages such as solvent-free conditions, excellent yields, simple procedure, mild conditions and reduced environmental consequences. The ionic liquid was recovered and reused. All of synthesized compounds were characterized by IR, NMR and elemental analyses.
author NIKPASSAND,MOHAMMAD
FEKRI,LEILA ZARE
AHMADI,PARVIN
author_facet NIKPASSAND,MOHAMMAD
FEKRI,LEILA ZARE
AHMADI,PARVIN
author_sort NIKPASSAND,MOHAMMAD
title GRINDING SYNTHESIS OF 2-AMINO-4H-CHROMENES USING 3,3-(BUTANE-1,4-DIYL) BIS (1,2-DIMETHYL- 1H-IMIDAZOLE-3-IUM)Br-CAN AS A NOVEL REAGENT
title_short GRINDING SYNTHESIS OF 2-AMINO-4H-CHROMENES USING 3,3-(BUTANE-1,4-DIYL) BIS (1,2-DIMETHYL- 1H-IMIDAZOLE-3-IUM)Br-CAN AS A NOVEL REAGENT
title_full GRINDING SYNTHESIS OF 2-AMINO-4H-CHROMENES USING 3,3-(BUTANE-1,4-DIYL) BIS (1,2-DIMETHYL- 1H-IMIDAZOLE-3-IUM)Br-CAN AS A NOVEL REAGENT
title_fullStr GRINDING SYNTHESIS OF 2-AMINO-4H-CHROMENES USING 3,3-(BUTANE-1,4-DIYL) BIS (1,2-DIMETHYL- 1H-IMIDAZOLE-3-IUM)Br-CAN AS A NOVEL REAGENT
title_full_unstemmed GRINDING SYNTHESIS OF 2-AMINO-4H-CHROMENES USING 3,3-(BUTANE-1,4-DIYL) BIS (1,2-DIMETHYL- 1H-IMIDAZOLE-3-IUM)Br-CAN AS A NOVEL REAGENT
title_sort grinding synthesis of 2-amino-4h-chromenes using 3,3-(butane-1,4-diyl) bis (1,2-dimethyl- 1h-imidazole-3-ium)br-can as a novel reagent
publisher Sociedad Chilena de Química
publishDate 2017
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072017000100019
work_keys_str_mv AT nikpassandmohammad grindingsynthesisof2amino4hchromenesusing33butane14diylbis12dimethyl1himidazole3iumbrcanasanovelreagent
AT fekrileilazare grindingsynthesisof2amino4hchromenesusing33butane14diylbis12dimethyl1himidazole3iumbrcanasanovelreagent
AT ahmadiparvin grindingsynthesisof2amino4hchromenesusing33butane14diylbis12dimethyl1himidazole3iumbrcanasanovelreagent
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