Alcohol to Mesylate using MsCl, base

Reaction, Reagents
& Mechanism

Reaction & Reagents info

Sulfonates as better leaving groups

  • Leaving group ability; OTf > OTs > OMs

Other ways of synthesizing better leaving groups for SN2 reactions:

    Stereochemical outcome of sulfonate ester (OMs, OTs and OTf):

    (a) Substitution:

    (b) Elimination:


    For review papers and other articles,
    refer to the tab "References"

    Useful Links on Reagent & Reaction:

    Mechanism

    Additional details

    Scheme & Procedure

    General Procedure:

    To a solution of alcohol (1 eq.) in dry DCM (10 Vol) at 0 oC was added triethylamine (1.5 eq.) followed by methanesulfonyl chloride (1.2 eq.) and stirred at 0 oC for 4 h (If the reaction does not proceed, it shall be brought to room temperature and stirred for 2 h). The reaction is monitored by TLC. After the completion of the reaction, the reaction mixture is diluted with water and layers separated. The aqueous layer is extracted with DCM. The organic layer is then successively washed with water (10 Vol x 2) and brine solution, dried over sodium sulphate, filtered and concentrated under reduced pressure to get the desired compound.

    Note:

    • The preferable solvents are DCM, toluene
    • Common bases are Pyridine, DIPEA, Et3N

    For more details on reactions and reagents,
    refer to the tab "Reaction, Reagents and Mechanism"

    Typical Procedure:

    For more details on large-scale reactions and OPRD procedures, 
    refer to the tab "Scale-up & Green Chem"

    WO2007121484, page No. 90

    WO2010045258, page No. 293

    Scale-up &
    Green Chem.

    Mesylates have been synthesized on large-scale and they are key intermediates in the manufacturing of pharmaceutical intermediates

    Scale-Up Typical Procedure:

    Green Chemistry Aspects:

    Reaction Tree

    References