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Methanesulfonic acid aryl esters

Fragmentation Loss of alkyl by fragmentation of the C-O bond with concomitant double H rearrangement to form the protonated sulfonic acid ion (m/z 97 for methanesulfonates), which then loses water. Loss of the alkoxyl residue (fragmentation of the S-O bond). Formation of an alkene ion from the sulfonate alkyl by a McLafferty-type rearrangement. In aryl esters, the phenoxy ion and the phenol radical cations dominate the spectrum. [Pg.425]


See other pages where Methanesulfonic acid aryl esters is mentioned: [Pg.359]    [Pg.155]    [Pg.236]    [Pg.269]    [Pg.236]    [Pg.730]    [Pg.95]   


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Aryl acid

Aryl esters

Esters arylation

Esters methanesulfonates

Methanesulfonate

Methanesulfonate esters

Methanesulfonic acid, acidity

Methanesulfonic esters

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