Transesterification of methylsulfate and ethylsulfate ionic liquids -
an environmentally benign way to synthesize long-chain and
functionalized alkylsulfate ionic liquids
A new environmentally friendly method to synthesize long-chain and
functionalized alkylsulfate ionic liquids is reported. The two-step
synthesis comprises the synthesis of a methylsulfate or
ethylsulfateionic liquid by direct alkylation in the first step. In the
second step, this intermediate is transformed in a transesterification
reaction, using different functionalized and nonfunctionalized
alcohols, to the corresponding new alkylsulfate melts. The entire
reaction sequence is halide-free and liberates methanol or ethanol as
the only by-products. Moreover, it is carried out in a solvent-free
manner and scale-up is straight forward.
%0 Journal Article
%1 ISI:000241036200013
%A Himmler, Simone
%A Hoermann, Stefanie
%A van Hal, Roy
%A Schulz, Peter S.
%A Wasserscheid, Peter
%D 2006
%J GREEN CHEMISTRY
%K Performance Synthesis and
%N 10
%P 887-894
%R 10.1039/b601583b
%T Transesterification of methylsulfate and ethylsulfate ionic liquids -
an environmentally benign way to synthesize long-chain and
functionalized alkylsulfate ionic liquids
%V 8
%X A new environmentally friendly method to synthesize long-chain and
functionalized alkylsulfate ionic liquids is reported. The two-step
synthesis comprises the synthesis of a methylsulfate or
ethylsulfateionic liquid by direct alkylation in the first step. In the
second step, this intermediate is transformed in a transesterification
reaction, using different functionalized and nonfunctionalized
alcohols, to the corresponding new alkylsulfate melts. The entire
reaction sequence is halide-free and liberates methanol or ethanol as
the only by-products. Moreover, it is carried out in a solvent-free
manner and scale-up is straight forward.
@article{ISI:000241036200013,
abstract = {{A new environmentally friendly method to synthesize long-chain and
functionalized alkylsulfate ionic liquids is reported. The two-step
synthesis comprises the synthesis of a methylsulfate or
ethylsulfateionic liquid by direct alkylation in the first step. In the
second step, this intermediate is transformed in a transesterification
reaction, using different functionalized and nonfunctionalized
alcohols, to the corresponding new alkylsulfate melts. The entire
reaction sequence is halide-free and liberates methanol or ethanol as
the only by-products. Moreover, it is carried out in a solvent-free
manner and scale-up is straight forward.}},
added-at = {2009-06-29T17:55:14.000+0200},
author = {Himmler, Simone and Hoermann, Stefanie and van Hal, Roy and Schulz, Peter S. and Wasserscheid, Peter},
biburl = {https://www.bibsonomy.org/bibtex/29d1374da4e551e896b8f8702cbdc41e8/psschulz},
doi = {{10.1039/b601583b}},
interhash = {02f7afcfe42efcca3c17870baaad7789},
intrahash = {9d1374da4e551e896b8f8702cbdc41e8},
issn = {{1463-9262}},
journal = {{GREEN CHEMISTRY}},
keywords = {Performance Synthesis and},
number = {{10}},
pages = {{887-894}},
timestamp = {2009-06-29T17:57:08.000+0200},
title = {{Transesterification of methylsulfate and ethylsulfate ionic liquids -
an environmentally benign way to synthesize long-chain and
functionalized alkylsulfate ionic liquids}},
unique-id = {{ISI:000241036200013}},
volume = {{8}},
year = {{2006}}
}