Retro-Friedel-Crafts-Type Acidic Ring-Opening of Triptycenes: A New Synthetic Approach to Acenes

The triptycene scaffold has been ring-opened by using a retro-Friedel-Crafts-type reaction under acidic conditions to give its corresponding anthrone product. 9-Hydroxytriptycenes and unsubstituted triptycene undergo ring-opening reaction under strongly acidic conditions, such as with TfOH. An investigation of the substitution effect has revealed that the electron-donating group on the arene moiety allows the reaction to proceed in the presence of a weaker acid, such as TFA. In addition, the reaction has been successfully applied toward the synthesis of tetracene.

Automated summary

The triptycene scaffold can be ring-opened through a retro-Friedel-Crafts-type reaction under acidic conditions, yielding the corresponding anthrone product. 9-Hydroxytriptycenes and unsubstituted triptycene undergo ring-opening reaction in strongly acidic conditions, such as with TfOH. The investigation of the substitution effect reveals that an electron-donating group on the arene moiety allows the reaction to proceed in the presence of a weaker acid, such as TFA. Additionally, the reaction has proven successful for the synthesis of tetracene.