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Zinc permanganate ethers

By far the most important oxidation of ethers is their conversion into esters and lactones. Only a few reagents are capable of such a transformation ozone [110], chromium trioxide [539, 586], zinc dichromate [660], potassium permanganate [855], zinc permanganate [898], benzyltriethylam-monium permanganate [902], and ruthenium tetroxide (which gives the best yields) [774, 940] (equations 324 and 325). [Pg.169]

DIEXHYLENE GLYCOL METHYL ETHER ACETATE (629-38-9) Combustible liquid (flash point 180°F/98°C). Moisture may cause decomposition with formation of acetic acid. Reacts violently with strong oxidizers, permanganates, peroxides, ammonium persulfate, bromine dioxide, calcium chlorate, chlorosulfonic acid, oleum, sulfuric acid, nitric acid, perchloric acid, and other strong acids. Incompatible with acyl halides, aliphatic amines, alkalis, boranes, isocyanates, nitrates. May form shock-sensitive mixtures with silver, cobalt, chlorinated hydrocarbons, nitromethane, chromium compounds. Attacks some plastics, rubber, and coatings. Attacks copper, brass, zinc. [Pg.417]

See other pages where Zinc permanganate ethers is mentioned: [Pg.236]    [Pg.236]    [Pg.36]    [Pg.236]    [Pg.61]    [Pg.262]    [Pg.10]    [Pg.844]    [Pg.57]    [Pg.57]    [Pg.61]    [Pg.795]    [Pg.694]    [Pg.4]    [Pg.844]    [Pg.844]    [Pg.262]    [Pg.844]    [Pg.262]    [Pg.73]    [Pg.374]    [Pg.288]    [Pg.339]    [Pg.137]    [Pg.327]    [Pg.341]    [Pg.348]    [Pg.561]    [Pg.698]    [Pg.764]    [Pg.783]    [Pg.807]    [Pg.25]    [Pg.32]    [Pg.128]    [Pg.147]    [Pg.633]    [Pg.636]    [Pg.858]    [Pg.878]    [Pg.914]    [Pg.946]    [Pg.950]    [Pg.951]   
See also in sourсe #XX -- [ Pg.236 , Pg.237 ]

See also in sourсe #XX -- [ Pg.236 , Pg.237 ]

See also in sourсe #XX -- [ Pg.7 , Pg.236 , Pg.237 ]

See also in sourсe #XX -- [ Pg.7 , Pg.236 , Pg.237 ]

See also in sourсe #XX -- [ Pg.236 , Pg.237 ]



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Zinc permanganate

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