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Fluorenone cyanohydrin

Traditionally cyanohydrins have been prepared by processes that require the establishment of an equilibrium between a ketone and its corresponding cyanohydrin. For many ketones, especially those that are sterically hindered, the position of the equilibrium is unsatisfactory for the effective synthesis of the cyanohydrin. We describe herein a general method for the synthesis of cyanohydrins which does not depend on an equilibrium process. As a result this synthetic procedure can be used to convert a wide variety of dialkyl, diaryl, and arylalkyl ketones into their corresponding cyanohydrins. In addition to the described conversion of benzophenone into its cyanohydrin, acetophenone, fluorenone, tert-butyl phenyl ketone, and a wide variety of aliphatic ketones have been converted into cyanohydrins by this general procedure (Table... [Pg.9]


See other pages where Fluorenone cyanohydrin is mentioned: [Pg.84]    [Pg.81]    [Pg.17]    [Pg.84]    [Pg.81]    [Pg.17]   
See also in sourсe #XX -- [ Pg.17 ]

See also in sourсe #XX -- [ Pg.17 ]

See also in sourсe #XX -- [ Pg.17 , Pg.60 ]




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Cyanohydrine

Cyanohydrins

Fluorenone

Fluorenones—

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