4-Toluenesulfonyl chloride → p-Toluenesulfonic acid

Participants

Reaction Steps

To a solution of the alcohol produced in Example XV in dry CH2C12 at 0 degree C. there were added triethylamine, p-toluenesulfonyl chloride and N,N-dimethyl-4-aminopyridine (catalytic amount). The mixture was stirred overnight at room temperature, and then diluted with ethyl acetate. The reaction mixture was washed with H2O, saturated aqueous NaHCO3 and brine solution, dried over Na2SO4, and concentrated in vacuo to a yellow oil. Purification by SiO2 column chromatography yielded the p-toluenesulfonate.

Provenance & Evidence