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Benzophenone-oxime

Bfflizophenone condenses with hydroxylamine hydrochloride in the presence of excess of sodium hydroxide solution to 3deld benzophenone oxime, m.p. 142° ... [Pg.729]

Beckmann rearrangement of benzophenone oxime to benz-anilide. Dissolve 2 g. of benzophenone oxime in 20 ml. of anhydrous ether in a small conical flask and add 3 g. of powdered phosphorus pentachloride (or 3 ml. of pure tbionyl chloride). Distil off the solvent and other volatile products on a water bath CAUTION ether), add 25 ml. of water, boil for several minutes and break up any lumps which may be formed. Decant the supernatant liquid, and recrystallise, in the same vessel, from boiling alcohol. The product is benzanilide, m.p. 163° confirm this by a mixed m.p. determination with an authentic specimen. [Pg.741]

Quinazoline 3-oxides were first prepared by Awers and von Meyen-burg in 1891 by the dehydration of o-acylamino benzophenone oximes with acetic acid-acetic anhydride and were assigned the in-dazole structure (33). This was then modified by Bischler to the... [Pg.276]

Beim 2,4-Dihydroxy-benzophenon-oxim kann durch potentialkontrollierte Reduktion (-0,7 V) an Quecksilber in 1 n Salzsaure mit etwas Athanol die Imin-Zwischenstufe als Hydrochlorid abgefangen werden7 (s. S. 699). [Pg.614]

Fig. 13. Dependence of half-wave potentials for the reduction of substituted benzenes on the total polar substituent constant, ax- Examples shown benzophenones [pH 0], benzophenone-oximes [pH 0], thiobenzophenones [pH 0], nitrobenzenes [pH 2-0], azo derivatives [pH 2-6]. (Taken from Zuman, 1969.)... Fig. 13. Dependence of half-wave potentials for the reduction of substituted benzenes on the total polar substituent constant, ax- Examples shown benzophenones [pH 0], benzophenone-oximes [pH 0], thiobenzophenones [pH 0], nitrobenzenes [pH 2-0], azo derivatives [pH 2-6]. (Taken from Zuman, 1969.)...
Nitrile oxide-BF3 complexes can also be used as electrophilic moieties with aromatic systems. Introducing BF3 into a mixture of 2,6-dichlorobenzonitrile oxide and mesitylene in hexane, gave 88% Z-2, 6 -dichloro-2,4,6-trimethyl-benzophenone oxime (128). [Pg.19]

Benzophenone, conversion to ethyl /S-hydroxy-0,0-diphenylpro-pionate, 44, 57 Benzophenone oxime, 44, 52 Benzopyrazole, 42, 69 3-Benzoylpropionic add, condensation with benzaldehyde to give a-benzylidene-y-phenyl-A y -bu-tenolide, 43, 3 N-Benzylacetamide, 42,18 n-Benzyiacrylamide, 42,16 Benzyl alcohol, reaction with acrylonitrile, 42,16... [Pg.55]

Scheme 22 Solid-phase synthesis of the biotinylated, farnesylated tetrapeptide (59) using the Kaiser benzophenone oxime resin. Scheme 22 Solid-phase synthesis of the biotinylated, farnesylated tetrapeptide (59) using the Kaiser benzophenone oxime resin.
A series of polystyrene-bound substituted benzophenone oximes 71a-d have been synthesized and tested by DeGrado and Kaiser as potential supports for the solid-phase preparation of protected peptide fragments (Scheme 38). ... [Pg.182]

C14H13NO 2-Hydroxy-5-mediyl-benzophenone oxime Photometric Mo 56... [Pg.533]

The 2,1,4-benzothiadiazepine (554) can be prepared by the cyclization of 5-chloro-2-(chloromethylsulfonylamino)benzophenone oxime in the presence of sodium methoxide. [Pg.645]

SPECTRA N-R Aniline Azobenzene Benzophenone oxime Benzylamine... [Pg.111]


See other pages where Benzophenone-oxime is mentioned: [Pg.729]    [Pg.741]    [Pg.741]    [Pg.1087]    [Pg.117]    [Pg.66]    [Pg.943]    [Pg.729]    [Pg.741]    [Pg.741]    [Pg.1087]    [Pg.126]    [Pg.131]    [Pg.97]    [Pg.344]    [Pg.555]    [Pg.126]    [Pg.63]    [Pg.404]    [Pg.218]    [Pg.69]    [Pg.731]    [Pg.103]    [Pg.103]    [Pg.69]    [Pg.729]    [Pg.741]    [Pg.741]    [Pg.1087]   
See also in sourсe #XX -- [ Pg.729 , Pg.741 ]

See also in sourсe #XX -- [ Pg.729 , Pg.741 ]

See also in sourсe #XX -- [ Pg.344 ]

See also in sourсe #XX -- [ Pg.729 , Pg.741 ]

See also in sourсe #XX -- [ Pg.353 ]

See also in sourсe #XX -- [ Pg.514 ]

See also in sourсe #XX -- [ Pg.729 , Pg.741 ]




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Benzophenone oxime Beckmann rearrangement

Benzophenone oxime reactions

Benzophenone oxime, 0-acyl

Benzophenone oxime, O-acyl

Benzophenone oxime, and Beckmann

Benzophenone oxime, and Beckmann rearrangement

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