|
[摘要]:During a Study of electrophilic aromatic addition reactions (Ad(E)Ar) to anthracene, anthryl ethers at the C9-position of anthracene were obtained as the major products when trans-9,10-dihydro-9,10-dimethoxyanthracene was reacted (10 minutes at 75 degrees C) with various alcohols. 9-Anthryl ethers with primary, secondary, cyclic alcohols, and polyethylene glycol (PEG) were isolated in 47-73% yields under optimized conditions. It is hoped that the devised method offers a new synthetic route for the preparation of anthryl ethers via the acid-catalyzed transetheritication of trans-9, 10-dihydro-9, 10-dimethoxyanthracene with various alcohols. |
|