Process for preparing a methyl-substituted benzaldehyde
AssigneeE. I. DuPont de Nemours and Company
InventorCarl A. Renner
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Abstract
Process for formylating an alkyl-substituted benzene using carbon monoxide and hydrogen chloride, in the presence of aluminum chloride catalyst, in a reaction mixture which includes chlorobenzene as a solvent, and process for oxidizing an alkyl-substituted benzaldehyde using oxygen, in the presence of an autoxidation initiator, in a reaction mixture which includes cyclohexanone as a reductant.
Claims6
Improved process for preparing a methyl-substituted benzoic acid by oxidizing, in a reaction mixture, at a temperature within the range about 0.degree. to 120.degree. C., the methyl-substituted benzaldehyde of the formula ##STR3## m is 2, 3, 4 or 5, with an excess of oxygen, in the presence of about 0.01 to 2 percent by weight, based on the weight of aldehyde, of an autoxidation initiator, with the methyl-substituted benzoic acid thus produced being separated from the reaction mixture and recovered, the improvement characterized in that the oxidation reaction is carried out in the reaction mixture in the presence of at least 0.5 molar equivalent, per mole of aldehyde, of cyclohexanone as a reductant.
Process of claim 1 wherein, upon substantial completion of the reaction, water is added to the reaction mixture to separate aluminum chloride from the aldehyde produced, the aqueous layer thus formed is removed and the residual aldehyde solution is used in the process of claim 5 as a source of the aldehyde.
Dependencies are inferred from the claim text.