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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378937Generated: November 3, 2026

Water → p-Toluenesulfonic acid

https://huagongshe.com/reaction/1378937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantPhenylisohexanolHCID 108312—
SolventDiethyl EtherHCID 3283—
Productp-Toluenesulfonic acidHCID 6101—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Phenoxanol (30.00 g, 0.168 mol) and pyridine (130 mL) are combined in a flask fitted with a condenser, internal thermometer, mechanical stirrer and argon inlet. The solution is cooled to -10° C. and to it is added p-toluenesulfonyl chloride (39.28 g, 0.202 tool) in portions via Gooch tubing so as to maintain the reaction temperature between -10°-0° C. After 3 h, water (20 mL) is added in portions so as to keep the temperature of the reaction below 5° C. The reaction mixture is warmed to room temperature and then poured into a separatory funnel containing 275 mL of ether. The layers are separated and the organic layer is washed with 5 M H2SO4 (75 mL), saturated CuSO4 solution (75 mL), water (2×75 mL) and saturated NaHCO3 solution (75 mL). After drying over MgSO4, the organic layer is filtered and concentrated to leave a light yellow liquid as phenoxanyl p-toluenesulfonate. Purity of the product is determined by thin layer chromatography and the structure confirmed by 1H and 13C NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670466
Source datasetuspto-grants-1997_09
ORD IDord-dabda240a0c341098615dd1e4d3c8854
Source noteuspto-grants-1997_09