The effects of reaction variables on the palladium-catalyzed reactions of butadiene with water
β Scribed by Byoung In Lee; Kyung Hee Lee; Jae Sung Lee
- Book ID
- 104421232
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 190 KB
- Volume
- 166
- Category
- Article
- ISSN
- 1381-1169
No coin nor oath required. For personal study only.
β¦ Synopsis
The effects of reaction variables on the reactions of butadiene with water in the presence of homogeneous palladium catalysts were investigated. The reactions in the presence of palladium, a phosphine ligand and carbon dioxide comprized telomerization, linear dimerization and cyclodimerization. The rate of reaction and the selectivity to 2,7-octadien-1-ol, 1,3,7-octatriene and 1-methylene 2-vinyl cyclopentane depended strongly upon the ratio of water to butadiene, the ratio of phosphine to palladium, the amount of carbon dioxide and the reaction time. 2,7-Octadien-1-ol that formed initially was subsequently converted to a mixture of 1,7-octadien-3-ol, 1,3,7-octatriene and 1-methylene-2-vinyl cyclopentane, the degree of which depended on the reaction conditions. A possible reaction pathway for the reaction of butadiene with water has been proposed.
π SIMILAR VOLUMES
Recently several reports have appeared concerning the reactions of butndiene with nucleophiles catalyzed by soluble palladium complexes (l-4).
Tertiary allylic amines react with butadiene in the presence of palladium(O) with cleavage of the carbon-nitrogen bond of the allylic amine and formation of the unsaturated tertiarv amine 4. - In the course of our studies of nickel-catalyzed additions of secondary amines to butadiene,2 we found th
## Abstract The aminoalcohols **1**, react with 2 equivalents of butadiene in the presence of catalytic quantities of bis (acetylacetonato)palladium/triphenylphosphine to give exclusively the corresponding __N__βoctadienyl amninoalcohols. In the presence of excess butadiene, subsequent __O__βoctadi