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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