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Esters, carboxylic acid saponification equivalent

The hydrolysis is generally not carried out at pH 7 but is either acid-catalyzed or base-mediated (i.e., as a so-called saponification). Base-catalyzed ester hydrolyses do not exist The carboxylic acid produced protonates a full equivalent of base and thus consumes it. [Pg.287]

In the second step, the two methyl ester moieties are hydrolyzed under basic conditions to the corresponding carboxylic acids. Whereas typical saponification methods (2 N KOH, reflux, 48 h) failed, the hydrolysis proceeded smoothly with "anhydrous hydroxide".This reagent - relatively unsolvated hydroxide - was generated via the reaction of two equivalents of potassium /er/-butoxide with one equivalent of water. [Pg.53]


See other pages where Esters, carboxylic acid saponification equivalent is mentioned: [Pg.185]    [Pg.49]    [Pg.1234]    [Pg.443]    [Pg.443]    [Pg.193]    [Pg.210]    [Pg.149]   
See also in sourсe #XX -- [ Pg.687 ]

See also in sourсe #XX -- [ Pg.687 ]




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Acid Saponification

Carboxylic equivalent

Carboxylic saponification

Ester saponification

Saponification

Saponification equivalent

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