A solvent-free synthesis of beta-enamino trihalomethyl ketones

An efficient green procedure to prepare a series of twenty-six 4-amino-1,1,1-trihalo-3-alken-2-ones [CX3C(O)CH=C(R¹)NR² R³, where X = F, Cl, R¹ = H, Me, and R²/R³ = H/Ph, H/4-F-Ph, H/Bn, H/(CH2)2OH, Me/Ph, Me/Bu, Et/Et, -(CH2)4-] from the solvent-free reaction of 1,1,1-trihalo-4-alkoxy-3-alken-2-ones with primary and secondary amines at room temperature for five minutes is reported (yields of 73-99%).

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Main Authors: Martins,Marcos A. P., Peres,Rodrigo L., Fiss,Gabriela F., Dimer,Frantiescoli A., Mayer,Rodrigo, Frizzo,Clarissa P., Marzari,Mara R. B., Zanatta,Nilo, Bonacorso,Helio G.
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Química 2007
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532007000800006
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spelling oai:scielo:S0103-505320070008000062008-02-12A solvent-free synthesis of beta-enamino trihalomethyl ketonesMartins,Marcos A. P.Peres,Rodrigo L.Fiss,Gabriela F.Dimer,Frantiescoli A.Mayer,RodrigoFrizzo,Clarissa P.Marzari,Mara R. B.Zanatta,NiloBonacorso,Helio G. solvent-free enaminones enones trihalomethyl-compounds green chemistry An efficient green procedure to prepare a series of twenty-six 4-amino-1,1,1-trihalo-3-alken-2-ones [CX3C(O)CH=C(R¹)NR² R³, where X = F, Cl, R¹ = H, Me, and R²/R³ = H/Ph, H/4-F-Ph, H/Bn, H/(CH2)2OH, Me/Ph, Me/Bu, Et/Et, -(CH2)4-] from the solvent-free reaction of 1,1,1-trihalo-4-alkoxy-3-alken-2-ones with primary and secondary amines at room temperature for five minutes is reported (yields of 73-99%).info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaJournal of the Brazilian Chemical Society v.18 n.8 20072007-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532007000800006en10.1590/S0103-50532007000800006
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language English
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author Martins,Marcos A. P.
Peres,Rodrigo L.
Fiss,Gabriela F.
Dimer,Frantiescoli A.
Mayer,Rodrigo
Frizzo,Clarissa P.
Marzari,Mara R. B.
Zanatta,Nilo
Bonacorso,Helio G.
spellingShingle Martins,Marcos A. P.
Peres,Rodrigo L.
Fiss,Gabriela F.
Dimer,Frantiescoli A.
Mayer,Rodrigo
Frizzo,Clarissa P.
Marzari,Mara R. B.
Zanatta,Nilo
Bonacorso,Helio G.
A solvent-free synthesis of beta-enamino trihalomethyl ketones
author_facet Martins,Marcos A. P.
Peres,Rodrigo L.
Fiss,Gabriela F.
Dimer,Frantiescoli A.
Mayer,Rodrigo
Frizzo,Clarissa P.
Marzari,Mara R. B.
Zanatta,Nilo
Bonacorso,Helio G.
author_sort Martins,Marcos A. P.
title A solvent-free synthesis of beta-enamino trihalomethyl ketones
title_short A solvent-free synthesis of beta-enamino trihalomethyl ketones
title_full A solvent-free synthesis of beta-enamino trihalomethyl ketones
title_fullStr A solvent-free synthesis of beta-enamino trihalomethyl ketones
title_full_unstemmed A solvent-free synthesis of beta-enamino trihalomethyl ketones
title_sort solvent-free synthesis of beta-enamino trihalomethyl ketones
description An efficient green procedure to prepare a series of twenty-six 4-amino-1,1,1-trihalo-3-alken-2-ones [CX3C(O)CH=C(R¹)NR² R³, where X = F, Cl, R¹ = H, Me, and R²/R³ = H/Ph, H/4-F-Ph, H/Bn, H/(CH2)2OH, Me/Ph, Me/Bu, Et/Et, -(CH2)4-] from the solvent-free reaction of 1,1,1-trihalo-4-alkoxy-3-alken-2-ones with primary and secondary amines at room temperature for five minutes is reported (yields of 73-99%).
publisher Sociedade Brasileira de Química
publishDate 2007
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532007000800006
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