Search results for "Methyl carbonate"
showing 6 items of 26 documents
Liquid–liquid equlibria of the system dimethyl carbonate+methanol+water at different temperatures
2006
Abstract In this work, experimental liquid–liquid equilibria (LLE) data of the dimethyl carbonate + methanol + water system are presented. The LLE of this system has been measured from 283 to 333 K. On the other hand, LLE and LVE of the binary system dimethyl carbonate + water have been measured. The equilibrium data presented are correlated using NRTL and UNIQUAC equations. The reliability of these models is tested by comparison with experimental results. Finally, the VLE for the system DMC + water at 101.3 kPa was predicted using the UNIQUAC model, with the adjusted parameters obtained from the LLE data. This prediction was successful when is compared with the experimental VLE data.
Direct electrochemical generation of organic carbonates by dehydrogenative coupling.
2018
Organic carbonates are an important source for polycarbonate synthesis. However, their synthesis generally requires phosgene, sophisticated catalysts, harsh reaction conditions, or other highly reactive chemicals. We present the first direct electrochemical generation of mesityl methyl carbonate by C–H activation. Although this reaction pathway is still challenging concerning scope and efficiency, it outlines a new strategy for carbonate generation.
1,3-Dimethylimidazolium-2-carboxylate: the unexpected synthesis of an ionic liquid precursor and carbene-CO2 adductElectronic supplementary informati…
2002
1,3-Dimethylimidazolium-2-carboxylate is formed in good yield, rather than the anticipated organic salt, 1,3-dimethylimidazolium methyl carbonate, as the reaction product resulting from both N-alkylation and C-carboxylation of 1-methylimidazole with dimethyl carbonate; the crystal structure of the zwitterion exhibits π-stacked rings and two-dimensional sheets constructed by hydrogen-bonds from imidazolium-ring hydrogens to the carboxylate group.
Linear Organic Carbonates
2003
The most common and successful method for producing organic carbonates, including polycarbonates, has been based for long time on the reaction between an alcohol or phenol and phosgene. The existing strict environmental regulations and the expanding market for organic carbonates do not assure that this technology can continue to have a leading role in this area, due to the inherent riskfulness of the processes. The market expansion of dimethyl carbonate (DMC), diphenyl carbonate (DPC), and bisphenol A polycarbonate (BPA-PC) is a reality, finding its driving force from the industrialization of alternative routes by EniChem (Italy) and UBE (Japan). This favorable situation can be foreseen for…
CO2 as a C1-Building Block for Dialkyl Carbonate Synthesis
2002
Carbon dioxide, one of the major man-made greenhouse gas, is a renewable resource of carbon which can be viewed as a C1 synthon to build valuable chemicals. The development of new applications is of major interest considering CO2 conversion and environmentally friendly reactions. As chemical catalysis offers interesting options, we are studying the molecular design of catalysts for the formation of dialkyl carbonates from alcohols and CO2. This paper reports results on the mechanistic approach for dialkyl carbonate formation with alkoxybutyl tin(IV) compounds. The insertion of CO2 into Sn-OR bonds (R = Me, 1Pr) occurs at atmospheric pressure and room temperature leading to alkylcarbonato ti…
Imidazolium-2-carboxylate as an afficient, expeditious and eco-friendly organocatalyst for glycerol carbonate synthesis
2009
An improved and greener approach towards the synthesis of glycerol carbonate, via transesterification, using 1-n-butyl-3-methylimidazolium-2-carboxylate as catalyst is described. The catalyst loading as low as 1% was sufficient to yield quantitative conversions. A plausible mechanism is proposed for the catalytic cycle leading to product formation.