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Synthesis of functionally substituted 2-cyanoacrylates

 

作者: T.I.Guseva,   N.G.Senchenya,   K.A.Mager,   V.A.Tsyryapkin,   Yu.G.Gololobov,  

 

期刊: Russian Chemical Bulletin  (Springer Available online 2004)
卷期: Volume 43, issue 4  

页码: 595-598

 

ISSN:1066-5285

 

年代: 2004

 

DOI:10.1007/BF00699831

 

出版商: Springer_US-Boston

 

数据来源: Springer

 

摘要:

The conditions for the Knoevenagel synthesis of 2-cyanoacrylates containing double and triple bonds in the alkoxycarbonyl group have been studied. It was found that the esters are formed in 10–70 % yields by the condensation of the respective cyanoacetates with formaldehyde in the 1∶1 ratio in the presence of piperidine, followed by the pyrolysis of the oligomers formedin vacuoat 170–200 °C in the presence ofpara-toluenesulfonic acid. The compounds synthesized readily undergo polymerization at room temperature and can be used as the basis for thermostable rapidly polymerizing adh

 

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