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Benzo phenone oxime

CbHiiNjO, 4 -Nitro-2.5.dimethoxy-benzo phenon.oxime 8 I 640. [Pg.962]

Schiff" bases derived from ketones have been rarely used one described example is the synthesis of cycloserine starting with benzo-phenone oxime... [Pg.764]

Ketoximes often give better yields in aq. NHg than in acid soln.— E Benzo-phenone oxime refluxed 4 hrs. with Zn-dust and NH4 acetate in aq. coned. NHg and ethanol -> henzhydrylamine. Y 91%. F. e. s. J. G. Jochims, M. 94, 677 (1963). [Pg.273]

Ii5c k /—v raw 208.25 crysts (from MeOH), mp 112° forms aa oxime, mp 197—98°, Prepn N-tosylanthranilyl chloride with m-xylene AlCa gives 2,4-methyl-2 -(tosyIamino)benzo-phenone which is saponified by sulfuric acid the product is diazotized with,NaN02 (Ref 3)... [Pg.233]

See other pages where Benzo phenone oxime is mentioned: [Pg.658]    [Pg.325]    [Pg.658]    [Pg.325]    [Pg.277]    [Pg.658]    [Pg.249]    [Pg.283]    [Pg.809]    [Pg.922]    [Pg.386]    [Pg.52]   
See also in sourсe #XX -- [ Pg.212 ]



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