Oxidative decarboxylation of cyclohexanecarboxylic acid
✍ Scribed by J. A. Bigot; P. L. Kerkhoffs
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 273 KB
- Volume
- 82
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
Cyclohexanecarboxylic acid is converted to a mixture of cyclohexanone and cyclohexene by reacting it at temperatures around 200° with an oxygen‐containing gas and steam in the presence of metal‐salt catalysts.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Molecules of the title compound, C 9 H 15 NO 3 , form a twodimensional hydrogen-bonded network, via O-HÁ Á ÁO and N-HÁ Á ÁO interactions, which runs parallel to the bc plane. In this structure, neither the carboxylic acid groups nor the carbamoyl groups are involved in dimer formations.