6044-68-4Relevant articles and documents
Process for producing a carboxylic acid ester by reacting an aldehyde and an alcohol using a palladium type catalyst
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Page column 4; 7-10, (2008/06/13)
A carboxylic acid ester is prepared by a process comprising: reacting an aldehyde and an alcohol in a liquid phase in the presence of molecular oxygen as indicated by the following reaction: RCHO+R′OH+O2→RCOOR′+H2O in the presence of a catalyst comprising at least palladium and an element X, wherein X is bismuth, lead or a combination thereof, supported on a carrier, wherein the catalyst has an acid strength, pKa, of more than 4.8 and shows an ammonia chemical adsorption amount at 0° C. of 0-150 μmol/g-catalyst.
INDIRECT ELECTROCHEMICAL α-METHOXYLATION OF ALIPHATIC ETHERS AND ACETALS - REACTIVITY AND REGIOSELECTIVITY OF THE ANODIC OXIDATION USING TRIS(2,4-DIBROMOPHENYL)AMINE AS REDOX CATALYST
Ginzel, Klaus-Dieter,Steckhan, Eberhard,Degner, Dieter
, p. 5797 - 5806 (2007/10/02)
The technically important α-methoxylation of aliphatic ethers and acetals to form mixed acetals respectively aldehydes or ortho-esters can be performed electrochemically at low potentials in methanol solution using an undivided cell and tris(2,4-dibromophenyl)amine as redox catalyst.The regioselectivity is usually considerably higher as compared with direct electrolysis in the abscence of a catalyst.Especially valuable is the method for the regioselective methoxylation of secondary carbon atoms in presence of primary or tertiary ones and of the acetal carbon in 1,3-dioxolanes.The redox catalyst is stable under the reaction conditions so that more than thousand turnovers could be obtained.