Synthesis of Epoxides Catalyzed by a Halide-Free Reaction-Controlled Phase-Transfer Catalytic System: [(CH3(CH2)17)2N(CH3)2]3[PW4O32]/H2O2/Dioxan/Olefin

2009 ◽  
Vol 62 (7) ◽  
pp. 739 ◽  
Author(s):  
Yong Ding ◽  
Baochun Ma ◽  
Dejie Tong ◽  
Hui Hua ◽  
Wei Zhao

The epoxidation of alkenes was successfully catalyzed by a recyclable catalytic system: [(CH3(CH2)17)2N(CH3)2]3[PW4O32]/H2O2/dioxan/olefin. This new catalytic system is not only capable of catalyzing homogeneous epoxidation of alkenes with a unique reaction-controlled phase-transfer character, but also avoids the use of chlorinated solvents. The reactions were conducted in a biphasic mixture of aqueous H2O2/dioxan, and many kinds of alkenes could be efficiently converted to the corresponding epoxides in high yields. Both new and used [(CH3(CH2)17)2N(CH3)2]3[PW4O32] catalyst was characterized by 31P magic angle spin NMR, and IR.

2009 ◽  
Vol 62 (8) ◽  
pp. 947 ◽  
Author(s):  
Yong Ding ◽  
Baochun Ma ◽  
Dejie Tong ◽  
Hui Hua ◽  
Wei Zhao

The epoxidation of alkenes was successfully catalyzed by a recyclable catalytic system: [(CH3(CH2)17)2N(CH3)2]3[PW4O32]/H2O2/dioxan/olefin. This new catalytic system is not only capable of catalyzing homogeneous epoxidation of alkenes with a unique reaction-controlled phase-transfer character, but also avoids the use of chlorinated solvents. The reactions were conducted in a biphasic mixture of aqueous H2O2/dioxan, and many kinds of alkenes could be efficiently converted to the corresponding epoxides in high yields. Both new and used [(CH3(CH2)17)2N(CH3)2]3[PW4O32] catalyst was characterized by 31P magic angle spin NMR, and IR.


Author(s):  
Xin Li ◽  
Guoliang Gao ◽  
Songtao He ◽  
Qiuling Song

Presented herein is the first 1,6-conjugate addition of diborylmethane, which is promoted by a simple and inexpensive copper catalytic system. This method features high yields, good selectivities and broad functional...


1997 ◽  
Vol 52 (20) ◽  
pp. 3511-3520 ◽  
Author(s):  
Tadaatsu Ido ◽  
Takanobu Yamamoto ◽  
Gong Jin ◽  
Shigeo Goto

Synthesis ◽  
2021 ◽  
Author(s):  
Michał Tryniszewski ◽  
Michal Barbasiewicz

A series of acyl fluorides was synthesized at 100 mmol scale using phase transfer catalyzed halogen exchange between acyl chlorides and aqueous bifluoride solution. The convenient procedure consists of vigorous stirring of the biphasic mixture at rt, followed by extraction and distillation. Isolated acyl fluorides (usually 7 g to 20 g) display excellent purity, and can be transformed into sterically hindered amides and esters, when treated with lithium amide bases and alkoxides under mild conditions.


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