A novel efficient protocol for preparation of 3-formyl-2-arylbenzo[b]furan derivatives

Abstract An efficient method for preparation of 3-formyl-2-arylbenzo[ b ]furan derivatives 4 from 3-chloro-2-(2-methoxyaryl)-1-arylprop-2-en-1-one 2 was developed, and the desired product was obtained in good to excellent yields. By converting 2-(2-methoxyphenyl)-3-oxo-3-phenylpropanal 1 to 2 , the regioselectivity problem occurring in the reaction when using 1 as the starting material was successfully avoided. Furthermore, a one-pot procedure for the successive demethylation, cyclization, and hydrolysis was evolved, although the intermediate 3-(dibromomethyl)-2-phenylbenzo[ b ]furan 3a could be isolated. A plausible mechanism was proposed based on some in situ investigations.