http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4262138-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-14
filingDate 1979-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1981-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ebcc4e067e2f085605c568dfbc9d484
publicationDate 1981-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4262138-A
titleOfInvention Preparation of carboxylic acid esters with BF3 complex catalyst
abstract In a process wherein ethylene or propylene is carbonylated with carbon monoxide to form carboxylic acid esters in the presence of a catalyst complex of one mole of BF3 and one mole of alcohol, the invention concerns a technique wherein the catalyst is recovered from the reaction product and recycled. The carbonylation is carried out until approximately one-half of the alcohol is consumed, to form a reaction mass containing the BF3, the alcohol, and the carboxylic acid ester in a 2:1:1 molar ratio. In the first step, the one mole of the free BF3 is vaporized from the reaction mass. The remaining admixture is a 1:1:1 mixture of the three aforesaid compounds. To this mixture additional alcohol is added and the mixture is subjected to distillation. A carboxylic acid ester/alcohol azeotrope and residual alcohol are removed by the distillation, to leave a residue containing a 1:2 BF3/alcohol complex. This complex is combined with an additional mole of BF3 to form the 1:1 catalyst complex used in the carbonylation. The additional mole of BF3 is preferably that initially separated from the reaction mass; however, it may be obtained from an external source. The carboxylic acid ester/alcohol mixture may be separated by azeotropic distillation using an azeotroping agent, such as octane, to recover the alcohol-octane as overhead product and the carboxylic acid ester as bottoms product.
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priorityDate 1979-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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