Investigating cyclic sotolon, maple furanone and their dimers in solution using optical rotation, electronic circular dichroism and vibrational circular dichroism

Abstract The experimental optical rotation (OR), electronic circular dichroism (ECD) and vibrational circular dichroism (VCD) spectra of ( R )-3-hydroxy-4,5-dimethylfuran-2(5H)-one (sotolon, 1 ) and ( R )-5-ethyl-3-hydroxy-4-methylfuran-2(5H)-one (maple furanone, 2 ) taken in chloroform were compared to their spectra calculated with time-dependent density functional theory (TDDFT). Sotolon was shown to exist as a dimer in chloroform while maple furanone remains a monomer. Transition state barriers for the enol/keto tautomerization of sotolon were calculated and found to be high. The VCD method offers promise to ultimately distinguish between the presence of monomers or dimers.