Abstract:
2,2,2-Trichloro-4-methoxy-1,3,2-benzodioxaphosphole reacts with arylacetylenes or 3-chloropropyne to give 2,7-dichloro-5-methoxy-4-aryl(haloalkyl)-1,2-benzoxaphosphinine 2-oxides. Hydrolysis of the latter leads to the opening of the oxaphosphinine ring and formation of (E)-2-(4-chloro-2- methoxy-6 hydroxyphenyl)ethenylphosphonic acid.
Citation:
A. V. Nemtarev, I. O. Nasibullin, R. R. Fayzullin, L. R. Grigor’eva, V. F. Mironov, “2,2,2-Trichloro-4-methoxy-1,3,2-benzodioxaphosphole in the reactions with terminal acetylenes”, Mendeleev Commun., 30:1 (2020), 34–37
Linking options:
https://www.mathnet.ru/eng/mendc1092
https://www.mathnet.ru/eng/mendc/v30/i1/p34
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