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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538629Generated: October 30, 2026

Hydrochloric Acid → (Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/538629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantMethylcyclohexaneHCID 7962—
ReactantSodium HydroxideHCID 14798—
Reactant(Oxan-4-yl)methanolHCID 2773573—
Solvent2-MethyltetrahydrofuranHCID 7301—
Product(Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonateHCID 1907757699%

Reaction Conditions

Temperature32.5 °C

Reaction Steps

To 97 g (810 mmol) of (tetrahydro-pyran-4-yl)-methanol in 2-methyltetrahydrofuran (190 mL) are added 165 mL of 50% aq. NaOH solution. To this stirred suspension is added dropwise with cooling a solution of p-toluene-sulfonylchloride (283 g, 1.46 mol) in 2-methyltetrahydrofuran (280 mL). The reaction is stirred at 30-35° C. for 18 h. The suspension is poured into a mixture of ice-water (280 mL) and aq. HCl solution (37%, 203 mL). After addition of methylcyclohexane (1.4 L) and further ice-water (0.2 L), the reaction mixture is stirred for 2 h in an ice-bath. The resulting crystalline precipitate is isolated by filtration and washed with methylcyclohexane (0.5 L) and water (0.5 L). Drying under reduced pressure at 40° C. gave 216 g of toluene-4-sulfonic acid tetrahydro-pyran-4-ylmethyl ester. Yield: 99%; ESI-MS: 271 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865744B1
Source datasetuspto-grants-2014_10
ORD IDord-8ea29db611614204bca07ed801ef6bb2
Source noteuspto-grants-2014_10