O-QUINONE METHIDE AS A COMMON INTERMEDIATE IN THE PYROLYSIS OF O-HYDROXYBENZYL ALCOHOL, CHROMAN AND 1,4-BENZODIOXIN

The product composition in the very low pressure pyrolysis (550-1210 K ) of o-hydroxybenzyl alcohol (HBA), 3,4-dihydro-2H-1-benzopyran (chrom an), and 1,4-benzodioxin (BD) indicates that o-quinone methide (o-QM) is the common intermediate in each case. At complete conversion of HBA , o-QM was observed as the only product and the mass spectrum of o-QM could be obtained. At higher temperatures (>950 K), o-QM is subsequent ly converted into benzene and CO. The thermolysis process for chroman starts with cleavage of the phenoxy-carbon bond and proceeds with ethe ne elimination, yielding o-QM, The high pressure rate parameters for u nimolecular decay have been determined to obey k(chroman)/s(-1) = 10(1 5.3) exp (-269/RT). For ED only the cleavage of the phenyl-vinoxy bond has been observed, and after rearrangement and CO elimination o-QM is formed. The Arrhenius equation for the overall rate of disappearance has been found as k(BD)/s(-1) = 10(15.6) exp (-310/RT). Ultimately (11 00 K) the thermolysis of BD leads to 1 mole of benzene and 2 moles of CO.