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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212071Generated: November 3, 2026

Thiophenol → HCID 15153910, compound

https://huagongshe.com/reaction/2212071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-1-butanolHCID 13569—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 15153910HCID 1515391079.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of thiophenol (5.02 ml, 49 mmol), 4-chloro-1-butanol (7.33 ml, 73.5 mmol) and potassium carbonate (20.32 g, 147 mmol) in acetonitrile (5 ml) was stirred at 60° C. for 18 hours. The cooled mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were concentrated in vacuo. The residue was dissolved in methanol (10 ml) and water (2 ml) and treated with Oxone™ (45.2 g, 73.5 mmol). The reaction was stirred at room temperature for 24 hours, then filtered and concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was concentrated to give an oil which was dissolved in dichloromethane (10 ml), treated with pyridinium p-toluenesulfonate (3.69 g, 14.7 mmol) and 3,4-dihydro-2H-pyran (13.35 ml, 147 mmol) and stirred at room temperature for 18 hours. The mixture was diluted with water and the layers separated. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel, eluting with 25% ethyl acetate/i-hexane, to yield the title compound as a clear oil (3.5 g, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101892B2
Source datasetuspto-grants-2006_09
ORD IDord-a77272f0eaa349b19c2484c104b97f5f
Source noteuspto-grants-2006_09