Synthesis and properties of 5-styryl-2-furancarboxylic acids

1981 ◽  
Vol 46 (11) ◽  
pp. 2724-2728 ◽  
Author(s):  
Viera Knoppová ◽  
Anton Beňo ◽  
Jaroslav Kováč

5-(4-X-Styryl)-2-furancarboxylic acids (X = H, Br, NO2, COOCH3, (CH3)2N) were prepared by oxidation of the appropriate 5-(4-X-styryl)-2-furaldehydes, or alternatively by alkaline hydrolysis of the corresponding methyl esters. The latter were obtained by reacting the 4-substituted benzaldehydes with 5-methoxycarbonylfuryltriphenylphosphonium chloride. The UV and IR spectra of products are commented. The apparent pK values of the synthesized acids were employed for calculation of the transmission coefficient π' through the benzene-furan system bridged by a -CH=CH- group.

1988 ◽  
Vol 53 (4) ◽  
pp. 822-832 ◽  
Author(s):  
Jiří Svoboda ◽  
Zuzana Kocfeldová ◽  
Jaroslav Paleček

Under conditions of phase-transfer catalysis or in homogeneous solution of potassium tert-butoxide the title compounds give stereoisomeric mixtures of substituted 2,3-epoxy nitriles III and IV. Alkaline hydrolysis of epoxy nitriles IV afforded the corresponding 2-arylpropanals in low yields. On treatment with methanol and potassium carbonate, epoxy nitriles III and IV were converted into epoxy esters in good yields.


1965 ◽  
Vol 38 (8) ◽  
pp. 1247-1253 ◽  
Author(s):  
Shigeru Oae ◽  
Naomichi Furukawa ◽  
Takao Watanabe ◽  
Yoshio Otsuji ◽  
Masayuki Hamada

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