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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-582
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C68-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C68-06
filingDate 1992-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c0b96dcebc0546774f55356037d64ef
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c20049ed334466100fc58661acb2d5dc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_541a59b53019f6b04c5a40df77b28f67
publicationDate 1992-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9218458-A1
titleOfInvention Continuous production process of diarylcarbonates
abstract A diaryl carbonate is produced by transesterification of a dialkyl carbonate, such as dimethyl carbonate, with an aromatic hydroxy compound, such as phenol, in three successive reaction zones. A transesterification catalyst, such as a titanate ester or ester mixture is used in each zone. Conditions are selected to maximise formation of alkyl aryl carbonate in the first and second reaction zones, whilst conversion to diaryl carbonate is favoured in the third reaction zone. The vaporous mixture from the first two reaction zones is a mixture containing alkyl alcohol, dialkyl carbonate, alkyl aryl carbonate and aromatic hydroxy compound. This mixture is separated in an alkyl alcohol recovery zone by distillation in the distillation columns to produce useful recycle streams. The second of these distillation columns can be operated at a lower pressure than the first, thus enabling the heat of vaporisation of this mixture to be used as the source of heat for the reboiler of the second distillation column of the alkyl alcohol recovery zone.
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