Summary
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1.
By reaction with diethylamine or piperidine, chlorodiphenylborine gives (diethylamino)diphenylborine or diphenylpiperidinoborine, respectively.
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2.
Chlorodiphenylborine reacts with ammonia at room temperature with formation of a chlorodiphenylborine-ammonia complex.
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3.
Diarylchloroborines from stable complex compounds with pyridine.
Literature cited
B.M. Mikhailov and T.A. Shchegoleva, Proc. Acad. Sci, USSR 108, 481 (1956).
B.M. Mikhailov and V.A. Vaver, Proc. Acad. Sci. USSR 109, 94 (1956).
B.M. Mikhailov and N.S. Fedotov, Bull. Acad. Sci. USSR, Div. Chem. Sci. 1956, 375.
B.M. Mikhailov and T.A. Shchegoleva, Bull. Acad. Sci. USSR, Div. Chem. Sci. 1956, 508.
B.M. Mikhailov and T.V, Kostroma, Bull. Acad. Sci. USSR, Div. Chem. Sci. 1956, 1144.
B.M. Mikhailov and T.V. Kostroma, Bull. Acad. Sci. USSR, Div. Chem. Sci. 1956, 376.
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Additional information
Communication 11, see [1]; Communication 13, see [2].
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Mikhailov, B.M., Fedotov, N.S. Organoboron compounds Communication 14. Action of organic bases on chlorodiphenylborine. Russ Chem Bull 5, 1561–1563 (1956). https://doi.org/10.1007/BF01177542
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DOI: https://doi.org/10.1007/BF01177542