1073-39-8

694-87-1

1073-39-8

The general procedure for the synthesis of 4-bromobenzocyclobutene from benzocyclobutene is as follows: first, α-chloro-o-xylene 1 is subjected to a pyrolysis reaction at about 800 °C and 0.5 mbar to produce benzocyclobutene 2 in 45% yield. Subsequently, benzocyclobutene 2 was dissolved in acetic acid and reacted with a mixture of bromine and iodine at room temperature for selective bromination to give 4-bromobenzocyclobutene 3. 3 was dissolved in toluene and a slightly molar excess of 1,4-dihydro-1,4-epoxynaphthalene 4 was added and reacted for 20 hr at 220° C. to give the Diels-Alder addition product 5 as a pure inner/outer in 80% yield mixture, which was a colorless crystalline substance. -yl)-5,12-dihydroanthracene 7. After recrystallization of compound 7 with o-dichlorobenzene, the dehydrogenation reaction was carried out by treatment with 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) in boiling o-xylene. After repeated vacuum sublimation purification, orange-red crystals of 2-(anthracen-2-yl)tetraphenyl 8 were finally obtained in 75% yield. All intermediates were characterized by 1H NMR, 13C NMR spectroscopy and mass spectrometry. Compound 8 was characterized by UV-visible spectroscopy.