Synthesis of dialkyl ethers by decarboxylation of dialkyl carbonates

The decarboxylation reaction of dialkyl carbonates to give their related ethers was investigated. The reaction was carried out at atmospheric pressure and in the presence of hydrotalcite or basic alumina as catalysts without any solvent. The influence of several reaction parameters on the selectivity was studied (e.g. temperature, amount of catalyst, substrate concentration, solvent). The stability of the catalyst was also investigated. The experimental data for the decarboxylation confirmed that this reaction is complicated by competitive processes, such as dismutation and, in one case, pyrolysis. The results obtained show that in the presence of hydrotalcite as a catalyst, symmetrical dialkyl ethers can be synthesised with yields up to 80%. Dissymmetrical ethers (i.e.methyl alkyl ethers) can be produced with yields up to 80% at high temperature (250 °C). The catalyst proved to be fully recyclable in all cases studied, except for the carbonate containing n-octyl moiety.

[1]  W. Su,et al.  Chemoselective Synthesis of Asymmetrical Carbonate from Alcohol and Dimethyl Carbonate Catalyzed by Ytterbium(III) Triflate , 2007 .

[2]  L. Rossi,et al.  Dimethyl carbonate as an ambident electrophile. , 2005, The Journal of organic chemistry.

[3]  P. Tundo,et al.  Direct synthesis of N-methylurethanes from primary amines with dimethyl carbonate , 2005 .

[4]  S. Memoli,et al.  Synthesis of methylethers by reaction of alcohols with dimethylcarbonate , 2004 .

[5]  L. Rossi,et al.  A safe and mild synthesis of organic carbonates from alkyl halides and tetrabutylammonium alkyl carbonates. , 2002, The Journal of organic chemistry.

[6]  A. Perosa,et al.  Selective mono-C-methylations of arylacetonitriles and arylacetates with dimethylcarbonate: a mechanistic investigation. , 2002, The Journal of organic chemistry.

[7]  M. Selva,et al.  Dimethylcarbonate for eco-friendly methylation reactions. , 2001, Chemosphere.

[8]  M. Selva,et al.  A Continuous-Flow O-Methylation of Phenols with Dimethyl Carbonate in a Continuously Fed Stirred Tank Reactor , 1999 .

[9]  M. Selva,et al.  Dimethyl Carbonate as a Methylating Agent. The Selective Mono-C-methylation of Alkyl Aryl Sulfones , 1997 .

[10]  M. Selva,et al.  Selective mono-N-methylation of primary aromatic amines by dimethylcarbonate over faujasite X- and Y-type zeolites , 1997 .

[11]  M. Selva,et al.  A new synthesis of 2-aryloxypropionic acids derivatives via selective mono-c-methylation of methyl aryloxyacetates and aryloxyacetonitriles with dimethyl carbonate , 1995 .

[12]  F. Trotta,et al.  Esters and orthoesters as alkylating agents at high temperature. Applications to continuous-flow processes , 1992 .

[13]  F. Trotta,et al.  Gas-liquid phase-transfer catalysis: a new continuous-flow method in organic synthesis , 1989 .

[14]  Pietro Tundo,et al.  Continuous-flow processes under gas-liquid phase-transfer catalysis (GL-PTC) conditions: the reaction of dialkyl carbonates with phenols, alcohols, and mercaptans , 1988 .

[15]  Yoshihiro Kobayashi,et al.  Reaction of dialkyltin dialkoxides with carbon disulfide at higher temperature. Preparation of orthocarbonates , 1971 .

[16]  R. Taylor Measurement of electrophilic aromatic reactivities via pyrolysis of 1-arylethyl acetates. Part V. Abnormal deactivation by some ortho-substituents: the direct field effect , 1971 .