Electrochemically site-selective alkoxylation of twisted 2-arylbenzoic acids via spirolactonization

The Electrochemical Cross-Dehydrogenative Coupling (ECDC) of twisted biphenyl-2-carboxylic acids with aliphatic alcohols provides 4 '-alkoxyspirolactones which isomerize, under mild basic conditions, to give 4 '-alkoxy-2-phenylbenzoic acids. This site-selective alkoxylation was readily adapted to 1 mmol scale and is environmentally friendly, as no terminal oxidants are needed and H-2 is the only residue. The suitability of diphenic acid derivatives in this two-step protocol is noteworthy, especially for axially chiral substrates that can be functionalized with retention of the configuration and of the enantiomeric purity. We have proposed a plausible mechanism based on experimental pieces of evidence that support the single-electron oxidation of the carboxylate, formed by deprotonation of the biphenyl-2-carboxylic acids with 2,6-lutidine, and DFT calculations that suggest a very fast spirocyclization of the intermediate sigma-aroyloxyl radical. Competing pathways to benzocoumarins were also examined by computational studies.

Automated summary

The ECDC method was utilized to synthesize 4'-alkoxyspirolactones and isomerize them into 4'-alkoxy-2-phenylbenzoic acids. This reaction is also suitable for axially chiral substrates, allowing for retention of configuration and enantiomeric purity.