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Synthesis of Azulene Derivatives
No.138(August 2009)

3,4-Dichlorothiophene 1,1-Dioxide (1) is useful as a synthetic starting material for the preparation of azulene derivatives. More specifically, the cycloaddition reaction of 1 with furan produce adducts 2 and 3, which can then be converted into 4 by treatment with triethylamine at room temperature. This compound 4 undergoes further cycloaddtion with 5 to give intermediate 6. Subsequent elimination of sulfur dioxide and dimethylamine affords 7 which can then be elaborated into azulene derivative 9 by treatment with tetrazine derivative 8, after denitrogenation and elimination of pyridazine derivative. Due to its instability, derivative 9 is isolated and identified as its Diels-Alder adduct with N-methylmaleimide.
References
- 1)The synthesis of some azuleno[c]furans
- 2)The synthesis of 5,6-dichloroazulene
- 3)Diels-Alder reactions and addition-rearrangement reactions of halogenated thiophene dioxides
Related Compounds
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