The Synthesis of Peashooter aromatic hydrocarbon
Keywords:
Peashooter aromatic hydrocarbon, bromination, benzocyclobutane, annulation, recarburizationAbstract
Peashooter aromatic hydrocarbon has a triple bond structure between benzene ring and carbon carbon, which can play a role in the polymer field. At the same time, it may have excellent performance, such as good conductivity and ductility, so it can be used in food industry, chemical industry, pharmaceutical industry and so on. A series of chemical reactions such as substitution reaction, reduction reaction and elimination reaction were used to design the synthesis steps of Peashooter aromatic hydrocarbon, hoping to perfectly present the memory of pea shooter.
References
Maiti, T. K.; Singh, J.; Majhi, J.; Ahuja, A.; Maiti, S.; Dixit, P.; Bhushan, S.; Bandyopadhyay, A.; Chattopadhyay, S. Polymer 2022, 255, 125151.
McIntee, O. M.; Welch, B. C.; Greenberg, A. R.; George, S. M.; Bright, V. M. Polymer 2022, 255, 125167.
Xu, M.; Liu, Y.; Pang, W.; Pan, Y.; Chen, M.; Zou, C.; Tan, C. Polymer 2022, 255, 125116.
Croce, T. A.; Hamilton, S. K.; Chen, M. L.; Muchalski, H.; Harth, E. Macromolecules 2007, 40, 6028-6031.
Meng, X.; Zhang, W.; Tan, Z.; Du, C.; Li, C.; Bo, Z.; Li, Y.; Yang, X.; Zhen, M.; Jiang, F.; Zheng, J.; Wang, T.; Jiang, L.; Shu, C.; Wang, C. Chem. Comm. 2012, 48, 425-427.
Rickborn, B. Textbook of Organic Reactions, Vol. 53, Eds:Leo, A., California, 1998, p. 250.
Brennführer, A.; Neumann, H.; Klaus, S.; Riermeier, T.; Almena, J.; Beller, Tetrahedron 2007, 63, 6252-6258.
Hemantha, H. P.; Sureshbabu, V. V. Org. Biomol. Chem. 2011, 9, 2597.
Kotha, S.; Halder, S.; Sreenivasachary, N. Arkivoc 2002, 2002, 21-27.
Jin, L.; Hao, W.; Xu, J.; Sun, N.; Hu, B.; Shen, Z.; Mo, W.; Hu, X. Chem. Comm. 2017, 53, 4124-4127.
