Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41231Generated: October 26, 2026

Water → Tetrahydrofuran-3-yl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/41231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant3-Furanol, tetrahydro-HCID 9960—
SolventEthyl AcetateHCID 8857—
SolventEthylacetate heptaneHCID 21899848—
ProductTetrahydrofuran-3-yl 4-methylbenzenesulfonateHCID 1383732567.5%

Reaction Steps

To a mixture of 3-hydroxytetrahydrofuran (7.00 g, 79.5 mmol) and pyridine (100 mL), was added p-toluenesulfonyl chloride (18.2 g, 95.4 mmol) while stirring at room temperature, and the resulting mixture was stirred for 8.5 hours. To the mixture, were added water and ethyl acetate. After thoroughly shaking the mixture, the organic layer was separated, and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The mixture was filtered, and then the solvent in the filtrate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate: n-heptane/ethyl acetate=4/1) to obtain the title compound (13.0 g, 53.7 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530504B2
Source datasetuspto-grants-2013_09
ORD IDord-872bb89e4f994941b3711d549ccabc83
Source noteuspto-grants-2013_09