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Ethers cleavage with acetyl tosylate

Methyltetrahydrofuran allowed to react 12hrs. at 25° with acetyl tosylate -> 1-acetoxypentyl 4-p-tosylate. Y 95%. - Catalysis by added Lewis acids is not necessary and cleavage of the most unreactive ethers occurs after a few hrs. reflux in acetonitrile. The cleavage of unsym. ethers favors a greater specificity than other methods. M. H. Karger and Y. Mazur, Am. Soc. 90, 3878 (1968). [Pg.43]


See other pages where Ethers cleavage with acetyl tosylate is mentioned: [Pg.21]    [Pg.33]    [Pg.646]    [Pg.1941]    [Pg.363]    [Pg.291]    [Pg.271]   
See also in sourсe #XX -- [ Pg.490 ]




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Ethers cleavage

Ethers cleavage with

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