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Triethyl oxonium borontrifluoride

Eqn. (a) shows the interaction of epichlorohydrin with boron trifluoride etherate in the presence of absolute methylene-chloride (CHgClg) to yield triethyl oxonium borontrifluoride (I). [Pg.273]

The reaction between 3-(p-Chlorophenyl) phthalimidine and triethyl oxonium borontrifluoride (I) is to be performed under absolute anhydrous condition with BFg to yield (II) by an abstraction of a mole of water. The product (II) being basic in character gets knocked out in an alkaline medium (NUgCOg-sat. soln.) and extracted successively with ether. [Pg.274]

How would you accomplish the synthesis of mazindoP starting from triethyl oxonium borontrifluoride and 3-(p-chlorophenyl) phthalimidine Explain. [Pg.275]

See other pages where Triethyl oxonium borontrifluoride is mentioned: [Pg.273]    [Pg.273]   
See also in sourсe #XX -- [ Pg.273 , Pg.274 ]



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2.4.5- Triethyl

BoronTrifluoride

Oxonium

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