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Synthesis of some derivatives of α-phenylethyl- and α-phenylisopropylboronic acids

  • N. V. Kruglova
  • R. Kh. Freidlina
Brief Communications
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Conclusions

  1. 1.

    The synthesis of theα-phenylethyl- andα-phenylisopropylmagnesium chlorides in THF at 0 to − 10° was described. Whenα-phenylisopropylmagnesium chloride is synthesized in THF at 20–45° it reacts with the THF to yield 5-methyl-5-phenyl-1-hexanol.

     
  2. 2.

    When reacted with methyl borate, theα-phenylethyl- andα-phenylisopropylmagnesium chlorides give theα-phenylethyl- andα-phenylisopropylboronic acids. We also prepared the anhydride ofα-phenylethylboronic acid and the diethanolamine esters ofα-phenylethyl- andα-phenylisopropylboronic acid.α-Phenylethylmercury chloride was obtained from the and mercuric chloride.

     

Keywords

Methyl Chloride Ester Anhydride Borate 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Literature cited

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Copyright information

© Consultants Bureau 1967

Authors and Affiliations

  • N. V. Kruglova
    • 1
  • R. Kh. Freidlina
    • 1
  1. 1.Institute of Heteroorganic CompoundsAcademy of Sciences of the USSRUSSR

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