
%0 Journal Article
%A Hishmat, OH 
%A Abd, el Rahman AH 
%T Reactions of substituted hydroxybenzofurans. III. Acylation of 5- and 6-Methoxy-2,3-diphenylbenzofurans
%J Australian Journal of Chemistry
%D 1974/11/01
%V 27
%N 11
%P 2499-2503
%K 
%R https://doi.org/10.1071/CH9742499
%U https://www.publish.csiro.au/paper/CH9742499 
%X Vilsmeier-Haack formylation of 5-methoxy-2,3-diphenylbenzofuran (1a) and 6-methoxy-2,3-diphenylbenzofuran(2a) gave the corresponding 6- formyl derivative (1b) and 5-formyl derivative (2b) respectively. Friedel-Crafts acetylation of (1a) and (2a) gave products of the same orientation. The aldehydes (1b), (2b) were converted by standard methods into the corresponding methyl ketones and substituted 2,3- diphenyl-6H-furo[2,3-g][1]benzopyran-6-ones and 2,3-diphenyl-7H- furo[3,2-g][1]-benzopyran-7-ones respectively. 
