K2CO3/PG DES promoted transition metal free room temperature synthesis of nitroaldols and nitroolefins

In this work, we have described the use of K2CO3/Propylene Glycol (PG) deep eutectic solvent (DES) as green and efficient alternative to volatile organic solvents for the formation of a very important reaction intermediate i.e., nitroaldols via Henry Reaction. Interestingly, the DES acted both as th...

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Main Authors: Parmita Phukan, Diganta Sarma
Format: Article
Language:English
Published: Elsevier 2022-01-01
Series:Current Research in Green and Sustainable Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666086522000017
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author Parmita Phukan
Diganta Sarma
author_facet Parmita Phukan
Diganta Sarma
author_sort Parmita Phukan
collection DOAJ
description In this work, we have described the use of K2CO3/Propylene Glycol (PG) deep eutectic solvent (DES) as green and efficient alternative to volatile organic solvents for the formation of a very important reaction intermediate i.e., nitroaldols via Henry Reaction. Interestingly, the DES acted both as the solvent as well as the catalyst without the assistance of external base, solvent and additive. Further, the obtained nitroaldol product was utilized for nitroolefin synthesis.
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spelling doaj.art-d4f0b3b1fa634ac4a4071e108c53487d2022-12-22T02:59:27ZengElsevierCurrent Research in Green and Sustainable Chemistry2666-08652022-01-015100259K2CO3/PG DES promoted transition metal free room temperature synthesis of nitroaldols and nitroolefinsParmita Phukan0Diganta Sarma1Department of Chemistry, Dibrugarh University, Dibrugarh, Assam, IndiaCorresponding author.; Department of Chemistry, Dibrugarh University, Dibrugarh, Assam, IndiaIn this work, we have described the use of K2CO3/Propylene Glycol (PG) deep eutectic solvent (DES) as green and efficient alternative to volatile organic solvents for the formation of a very important reaction intermediate i.e., nitroaldols via Henry Reaction. Interestingly, the DES acted both as the solvent as well as the catalyst without the assistance of external base, solvent and additive. Further, the obtained nitroaldol product was utilized for nitroolefin synthesis.http://www.sciencedirect.com/science/article/pii/S2666086522000017Green chemistryNitroaldolsNitroolefinsMetal-freeRoom temperature
spellingShingle Parmita Phukan
Diganta Sarma
K2CO3/PG DES promoted transition metal free room temperature synthesis of nitroaldols and nitroolefins
Current Research in Green and Sustainable Chemistry
Green chemistry
Nitroaldols
Nitroolefins
Metal-free
Room temperature
title K2CO3/PG DES promoted transition metal free room temperature synthesis of nitroaldols and nitroolefins
title_full K2CO3/PG DES promoted transition metal free room temperature synthesis of nitroaldols and nitroolefins
title_fullStr K2CO3/PG DES promoted transition metal free room temperature synthesis of nitroaldols and nitroolefins
title_full_unstemmed K2CO3/PG DES promoted transition metal free room temperature synthesis of nitroaldols and nitroolefins
title_short K2CO3/PG DES promoted transition metal free room temperature synthesis of nitroaldols and nitroolefins
title_sort k2co3 pg des promoted transition metal free room temperature synthesis of nitroaldols and nitroolefins
topic Green chemistry
Nitroaldols
Nitroolefins
Metal-free
Room temperature
url http://www.sciencedirect.com/science/article/pii/S2666086522000017
work_keys_str_mv AT parmitaphukan k2co3pgdespromotedtransitionmetalfreeroomtemperaturesynthesisofnitroaldolsandnitroolefins
AT digantasarma k2co3pgdespromotedtransitionmetalfreeroomtemperaturesynthesisofnitroaldolsandnitroolefins