Transmission of polar effects. Part 16. Ionisation of 8-substituted 1-naphthoic acids and the alkaline hydrolysis of their methyl esters

Author(s):  
Socrates Acevedo ◽  
Keith Bowden
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.


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

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