Hydroformylation and hydroalkylcarbonylation of 3,4-dihydro[2H]pyran catalysed by Co2(CO)8 under syngas conditions

被引:6
作者
Arias, Jose L. [1 ]
Sharma, Pankaj [2 ]
Cabrera, Armando [2 ]
Beristain, Fernando [1 ]
Sampere, Rafael [1 ]
Arizmendi, Cesar [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Estudios Super Cuautitlan, Dept Quim, Cuautitlan 54700, Estado De Mexic, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Quim, Mexico City 04510, DF, Mexico
关键词
GAS-SHIFT REACTION; RHODIUM; OLEFINS; SYSTEM; ETHERS; H2O; CO;
D O I
10.1007/s11243-013-9750-4
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In the cobalt-catalysed hydroformylation of 3,4-dihydro[2H]pyran, the influence of different reaction parameters such as time, pressure, triphenylphosphine addition, catalyst and substrate concentration has been investigated. 2-formyl-tetrahydropyran, tetrahydropyran and a hydroalkylcarbonylation product were the main reaction products. The selectivity towards 2-formyl-tetrahydropyran formation is favoured at constant catalyst and substrate concentration. The coordination of the pyran's oxygen to the cobalt atom seems to be an important intermediate for the formation of 2-formyl-tetrahydropyran. Different substrate or catalyst concentrations promote the formation of other reduced products. The addition of triphenylphosphine to the catalyst leads to a less active species, which decreases the yield and promotes the hydroalkylcarbonylation reaction.
引用
收藏
页码:787 / 792
页数:6
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