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10.3: Alcohol conversion to Esters - Tosylate and Carboxylate

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    The poor leaving group of alcohols can be overcome by converting the hydroxyl group to a tosylate ester, an excellent leaving group. The tosylate ester undergoes subsequent reactions (typically SN1 or SN2) as part of a multiple step synthesis.

    ROH to tosylate to many different cpds.png

    The synthesis of carboxylate esters (the other ester) is commonly the final step of a synthetic pathway.

    Tosylate Ester Formation

    We can transform an alcohol group into a sulfonic ester using para-toluene sulfonyl chloride (Ts-Cl) or methanesulfonyl chloride (Ms-Cl), creating what is termed an organic tosylate or mesylate:



    Notice that unlike the halogenation reactions of alcohols with thionyl chloride or phosphorous tribromide, conversion of an alcohol to a tosylate or mesylate proceeds with retention of configuration at the electrophilic carbon.

    Tosylate/mesylate groups are excellent leaving groups in nucleophilic substitution reactions, due to resonance delocalization of the developing negative charge on the leaving oxygen.


    The laboratory synthesis of isopentenyl diphosphate - the 'building block' molecule used by nature for the construction of isoprenoid molecules such as cholesterol and b-carotene - was accomplished by first converting the alcohol into an organic tosylate (step 1), then displacing the tosylate group with an inorganic pyrophosphate nucleophile (step 2) (J. Org. Chem 1986, 51, 4768).


    The major reactive species of tosylate chemistry are summarized below.

    tosylate language.png



    4. Predict the structures of A and B in the following reaction.




    ch 12 sect 3 exercise answer.png


    Conversion of Alcohols into Esters

    Acid chlorides react with alcohols to form esters


    Example \(\PageIndex{1}\)



    5. Predict the products or specify the reagents for the following reactions.

    ch 12 sect 3 exerise 5.png



    ch 12 sect 3 exerise 5 solution.pngalt

    Contributors and Attributions

    Organic Chemistry With a Biological Emphasis by Tim Soderberg (University of Minnesota, Morris)


    10.3: Alcohol conversion to Esters - Tosylate and Carboxylate is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by LibreTexts.

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