Oxidative coupling of amines and carbon monoxide catalyzed by palladium complexes. Mono- and double carbonylation reactions promoted by iodine compounds
Abstract
<jats:p> Iodine is an effective promoter for the carbonylation of primary and secondary amines to ureas using palladium acetate as the catalyst and a base (e.g. K<jats:sub>2</jats:sub>CO<jats:sub>3</jats:sub>) in acetonitrile (3 h at 95 °C and 2.7 atm). Oxamides are formed in excellent yields when secondary amines are carbonylated in the presence of iodide ion and oxygen, while primary amines give ureas as the principal product at 95 °C, and oxamide at room temperature. Keywords: oxamides, ureas, double carbonylation, amines. </jats:p>
Journal
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- Canadian Journal of Chemistry
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Canadian Journal of Chemistry 68 (9), 1544-1547, 1990-09-01
Canadian Science Publishing
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Keywords
Details 詳細情報について
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- CRID
- 1364233269300014848
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- NII Article ID
- 30021730358
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- DOI
- 10.1139/v90-238
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- ISSN
- 14803291
- 00084042
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- Data Source
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- Crossref
- CiNii Articles