Mechanistic Insights into the B(C₆F₅)₃‑Initiated Aldehyde–Aniline–Alkyne Reaction To Form Substituted Quinolines

A substoichiometric quantity of the Lewis acid B­(C6F5)3 is sufficient to initiate the aldehyde–amine–alkyne reaction, in a one-pot methodology that enables the synthesis of a range of functionalized quinolines. Optimization studies revealed that key requirements for the high-yielding tricomponent reaction initiated by B­(C6F5)3 at raised temperatures include an excess of the in situ generated imine (which acts as a hydrogen acceptor) and an alkyne substituent able to stabilize positive charge buildup during the cyclization. Mechanistic experiments revealed that under these conditions B­(C6F5)3 is acting as a Lewis acid-assisted Brønsted acid, with H2O–B­(C6F5)3 being the key species enabling catalytic quinoline formation. This was indicated by deuterium labeling studies and the observation that the cyclization of N-(3-phenylpropargyl)­aniline using B­(C6F5)3 under anhydrous conditions afforded the zwitterion [(N-H-3-B­(C6F5)3-4-Ph-quinolinium], which does not undergo protodeboronation to release B­(C6F5)3 and the quinoline product under a range of conditions. Finally, a brief substrate scope exploration demonstrated that this is an operationally simple and effective methodology for the production of functionalized quinolines.