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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467136Generated: October 26, 2026

Thiophenol → 2-(Phenylthio)thiophene

https://huagongshe.com/reaction/467136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantThiopheneHCID 8030—
ReactantChlorosuccinimideHCID 31398—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418439HCID 178418439—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
Product2-(Phenylthio)thiopheneHCID 2778915—

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a suspension of N-chlorosuccinimide (7.8 g) in benzene (30 ml) was added dropwise, a solution of thiophenol (5.51 g) in benzene (20 ml) at room temperature. After 1 hour, the suspension was filtered, the filter pad washed with benzene and the filtrate evaporated under reduced pressure to give an orange oil. The oil was dissolved in dry tetrahydrofuran (20 ml) and added dropwise to a solution of 2-thienyl-lithium (prepared by the addition of n-butyllithium (20 ml, 2.5M) to thiophene (4.2 g) in dry tetrahydrofuran (30 ml) at -15° C. under nitrogen and stirred for 2 hours) at -15° C. under N2. The solution was stirred for 1 hour, allowed to warm to room temperature and stirred overnight. The reaction mixture was poured on to ice, extracted with ether (3×100 ml), dried over MgSO4 and evaporated under reduced pressure to give a brown oil. The oil was flash chromatographed on a Sorbsil C60-40/60H column using petroleum ether (40°-60° C.) to give a colourless oil, b.p. 161° C./20 mm pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158971
Source datasetuspto-grants-1992_10
ORD IDord-c351123020024690a3ebc4e0d69322dc
Source noteuspto-grants-1992_10