Catalyst concentration effect on the hydroesterification and hydroformylation-acetalization of 1-hexene by a Rh complex

被引：6

作者：

Hung-Low, Fernando

Uzcategui, Gabriela C.

Alvarez, Juan

Ortega, Marisol C.

Pardey, Alvaro J. ^{[1
]}

Longo, Clementina

机构：

[1] Cent Univ Venezuela, Fac Ciencias, Escuela Quim, Ctr Equilibrios Soluc, Caracas, Venezuela

[2] Cent Univ Venezuela, Fac Farm, Ctr Invest & Desarrollo Radiofarmacos, Caracas, Venezuela

来源：

REACTION KINETICS AND CATALYSIS LETTERS | 2006年 / 88卷 / 01期

关键词：

hydroesterification; methyl-heptanoate; 1-hexene; rhodium;

D O I：

10.1007/s11144-006-0127-y

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

The complex, [Rh(COD)(4-picoline)(2)](PF6) (COD=1,5-cyclooctadiene), immobilized on poly(4-vinylpyridine) in contact with methanol catalyzes the hydroesterification and hydroformylation-acetalization of 1-hexene to methylheptanoate, heptanal and 1,1-dimethoxyheptane, respectively. The by-product, 1,1-dimethoxyheptane comes from the nucleophilic addition of methanol over the heptanal formed. Also, H, and CO, from the water gas shift reaction (WGSR) are observed. The catalytic activity for the hydroformylation and the WGSR proved to be non-linear in the rhodium total concentration range 0.9-5.0 wt.%.

引用

页码：143 / 148

页数：6

共 6 条

[1] Selective hydroformylation-acetalization of aryl alkenes in methanol catalyzed by RhCl3•3H2O-P(OPh)3 system [J].