Optimised microwave-assisted synthesis of methylcarbonate salts: a convenient methodology to prepare intermediates for ionic liquid libraries
The reaction of 1-butylpyrrolidine with dimethyl carbonate to yield the ionic liquid precursor, 1-butyl-1-methylpyrrolidinium methylcarbonate, has been investigated under microwave heating conditions and the reaction parameters optimised to achieve 100% yield of the pyrrolidinium salt with no by-...
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Royal Chemical Society
2010
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my.utp.eprints.78272017-01-19T08:24:36Z Optimised microwave-assisted synthesis of methylcarbonate salts: a convenient methodology to prepare intermediates for ionic liquid libraries C.D., Wilfred Holbrey, John QD Chemistry The reaction of 1-butylpyrrolidine with dimethyl carbonate to yield the ionic liquid precursor, 1-butyl-1-methylpyrrolidinium methylcarbonate, has been investigated under microwave heating conditions and the reaction parameters optimised to achieve 100% yield of the pyrrolidinium salt with no by-products in under 1 h. The reactions of tributylamine, trioctylphosphine, and 1-butylimidazole with dimethyl carbonate under comparable conditions have also been evaluated, yielding the corresponding methylcarbonate salts which can be used as intermediates for the preparation of halide-free ionic liquids without generating any undesirable salt wastes. Royal Chemical Society 2010 Article PeerReviewed text/html http://eprints.utp.edu.my/7827/1/Holbrey.pdf application/pdf http://eprints.utp.edu.my/7827/2/Holbrey.pdf C.D., Wilfred and Holbrey, John (2010) Optimised microwave-assisted synthesis of methylcarbonate salts: a convenient methodology to prepare intermediates for ionic liquid libraries. Green Chemistry, 12 . pp. 407-413. http://eprints.utp.edu.my/7827/ |
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QD Chemistry C.D., Wilfred Holbrey, John Optimised microwave-assisted synthesis of methylcarbonate salts: a convenient methodology to prepare intermediates for ionic liquid libraries |
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The reaction of 1-butylpyrrolidine with dimethyl carbonate to yield the ionic liquid precursor,
1-butyl-1-methylpyrrolidinium methylcarbonate, has been investigated under microwave heating
conditions and the reaction parameters optimised to achieve 100% yield of the pyrrolidinium salt
with no by-products in under 1 h. The reactions of tributylamine, trioctylphosphine, and
1-butylimidazole with dimethyl carbonate under comparable conditions have also been evaluated,
yielding the corresponding methylcarbonate salts which can be used as intermediates for the
preparation of halide-free ionic liquids without generating any undesirable salt wastes. |
format |
Article |
author |
C.D., Wilfred Holbrey, John |
author_facet |
C.D., Wilfred Holbrey, John |
author_sort |
C.D., Wilfred |
title |
Optimised microwave-assisted synthesis of methylcarbonate salts: a
convenient methodology to prepare intermediates for ionic liquid libraries |
title_short |
Optimised microwave-assisted synthesis of methylcarbonate salts: a
convenient methodology to prepare intermediates for ionic liquid libraries |
title_full |
Optimised microwave-assisted synthesis of methylcarbonate salts: a
convenient methodology to prepare intermediates for ionic liquid libraries |
title_fullStr |
Optimised microwave-assisted synthesis of methylcarbonate salts: a
convenient methodology to prepare intermediates for ionic liquid libraries |
title_full_unstemmed |
Optimised microwave-assisted synthesis of methylcarbonate salts: a
convenient methodology to prepare intermediates for ionic liquid libraries |
title_sort |
optimised microwave-assisted synthesis of methylcarbonate salts: a
convenient methodology to prepare intermediates for ionic liquid libraries |
publisher |
Royal Chemical Society |
publishDate |
2010 |
url |
http://eprints.utp.edu.my/7827/1/Holbrey.pdf http://eprints.utp.edu.my/7827/2/Holbrey.pdf http://eprints.utp.edu.my/7827/ |
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1738655606025224192 |
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13.160551 |