The improved method for the efficient tosylation of alcohols has been reported using two procedures (A and B). Procedure A:
methanol, ethanol, benzyl alcohols, and valuable ethylene glycols can be converted into their corresponding alkyl tosylates in very fast,
simple, and efficient grinding method using potassium carbonate as solid base. Other primary and secondary alcohols need to add potassium
hydroxide to reaction mixture (procedure B). High selectivity of tosylation was observed for these two procedures. Scale up ability was found
in this method even in 100 mmol of substrate. The present method is the example of solid-state tosylation using tosyl chloride, and is a green
chemical process due to solvent-free conditions.
