Abstract
Complete silylation of all hydroxyl groups of hydroxyquinones is reported to be effectively carried out using N-methyl-N-trimethylsilyl-trifluoroacetamide (MSTFA). The silylated products are studied by gas chromatography/mass spectrometry. A detailed study of their mass spectra provides data for the elucidation of their fragmentation mechanisms as well as the deduction of the hydroxy-group position in the hydroxyquinone backbone.