RHODIUM-CATALYZED SYNTHESIS OF 2(5H)-FURANONES FROM TERMINAL ALKYNES AND NON-SUBSTITUTED ALKYNES UNDER WATER-GAS SHIFT REACTION CONDITIONS

被引:23
作者
JOH, T
NAGATA, H
TAKAHASHI, S
机构
[1] The Institute of Scientific and Industrial Research, Ibaraki, Osaka, 567, Osaka Universiry
关键词
CATALYSIS; FURANONE; OXYGENATE COMPOUNDS; RHODIUM COMPLEXES; ALKYNE COMPLEXES;
D O I
10.1016/0020-1693(94)03853-8
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Rhodium-catalyzed synthesis of 2(5H)-furanones from alkynes under water-gas shift reaction conditions was studied. By improving the reaction conditions for internal alkynes reported previously, the reaction could be extended to terminal alkynes. Terminal alkynes are selectively converted into 3- and 4-substituted 2(5H)-furanones (2 and 3). When acetylene itself is used, 2(5H)-furanone (2n) is obtained in a good yield. Examination of reaction solutions by IR spectroscopy and some other experimental findings suggest that the active species would be an alkyne-coordinated monomeric rhodium anion. A new reaction path is proposed.
引用
收藏
页码:45 / 53
页数:9
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