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Acetic Anhydride oxidation

Chloro-1 -dihvdro-5-phenvl-2H-1,4-benzodiazepin-2-one-4-oxide Acetic anhydride Sodium hydroxide... [Pg.1130]

Triflouroacetic anhydride was used before oxalyl chloride and is also known as the Swern Oxidation. Acetic anhydride can also be used. (Albright-Goldman Oxidation)... [Pg.638]

Epoxide formation is nearly suppressed when massively subeti-tuted olefine, such as 2,2,4-trimethyl-3-hexene among others, ate subjected to the chromic oxide-acetic anhydride reagent,42 Cyclo-hexene yields primarily 2-cyclohexenone and cyclohexane- 1,2-dione777 although some cyclohexane oxide appears to bo formed also (Eq, 111). [Pg.367]

Albright-Goldman Oxidation (Acetic Anhydride-Mediated Moffatt Oxidation)... [Pg.113]

OXIDATION, REAGENTS Dimethylsulf-oxide-Acetic anhydride. 1-Amyl hydroperoxide. N-Bromosuccinimide. Ceric ammonium nitrate. Chloramine. o-Chlo-ranil. 1-Chlorobenzotriazole. N-Chloro-succinimide-Dimethyl Sulfide. Chromic acid. Chromic anhydride. Chromyl chloride. Cobalt(ll) acetate. Cupric acetate monohydrate. Cupric nitrate-Pyridhic complex. 2,3-Dichloro-5,6-dicyano-l, 4-benzoquinonc. Dicyclohcxyl-18-crown-... [Pg.586]

Propylene oxide Butylene oxide Acetic anhydride... [Pg.203]

GLICERINA (Spanish) (56-81-5) Combustible liquid (flash point 390°F/199°C). Violent reaction with strong oxidizers, acetic anhydride, calcium hypochloride, chlorine, chromic anhydride, chromium oxide, ethylene oxide, hydrogen peroxide, phosphorus triiodide, potassium permanganate, potassium peroxide, silver perchlorate, sodium hydride, sodium peroxide, sodium triiodide, sodium tetrahydroborate. Incompatible with strong acids, caustics, aliphatic amines, isocyanates, uranium fluoride. Able to polymerize above 293°F/145°C. [Pg.599]

KP03)3-II was first prepared by Grunze and co-workers (24). When potassium dihydrogen orthophosphate is treated with a mixed solution of acetic acid and diacetyl oxide (acetic anhydride) at 90°C. for 24 hr., almost all of it is converted into crystalline potassium trimetaphosphate (KP03)3-II. [Pg.233]

Careful temperature control is especially important in this case, since lead tetraacetate is hydrolyzed at higher temperatures by the water formed in the reaction. When acetic anhydride is used, temperature control is still necessary because lead tetraacetate oxidizes acetic anhydride above 65°-70°. [Pg.139]

See other pages where Acetic Anhydride oxidation is mentioned: [Pg.286]    [Pg.121]    [Pg.197]    [Pg.197]    [Pg.306]    [Pg.143]    [Pg.286]    [Pg.521]    [Pg.529]    [Pg.560]    [Pg.900]    [Pg.1046]    [Pg.30]    [Pg.114]    [Pg.129]    [Pg.193]    [Pg.566]    [Pg.600]    [Pg.622]    [Pg.631]    [Pg.631]    [Pg.634]    [Pg.636]    [Pg.1134]    [Pg.137]    [Pg.406]   
See also in sourсe #XX -- [ Pg.2 ]



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2,5-Dimethylpyrazine 1-oxide with acetic anhydride

3-Methoxycarbonylpyrazine 1-oxide with acetic anhydride

Acetalization-oxidation

Acetals oxidation

Acetate oxidation

Acetic anhydride DMSO oxidation of alcohols

Acetic anhydride, trifluoroactivator DMSO oxidation of alcohols

Acetic oxide

Glucose, acetic anhydride reaction oxidation

Methylpyrazine 1-oxides with acetic anhydride

Primary alcohol oxidations acetic anhydride

Pyridine 1-oxide reaction with acetic anhydride

Tertiary amine oxides, Polonovski reactions, acetic anhydride

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