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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713276Generated: October 25, 2026

Thiophenol → 2-(Phenylthio)benzaldehyde

https://huagongshe.com/reaction/1713276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzaldehydeHCID 68023—
Solvent1,3-Dimethyl-2-imidazolidinoneHCID 6661—
Product2-(Phenylthio)benzaldehydeHCID 12340685—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 4-fluorobenzaldehyde (0.443 mL) in 1,3-dimethyl-2-imidazolidinone (6.4 mL) was added potassium carbonate (0.659 g). Then benzenethiol (0.326 mL) was added, and the resulting mixture was stirred at 120° C. for 2.5 hours. The reaction mixture was cooled to room temperature and then partitioned between diethyl ether (60 mL) and water (15 mL). The organic layer was washed successively with water (15 mL×2) and brine (15 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound (0.826 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795236B2
Source datasetuspto-grants-2010_09
ORD IDord-daa6ad5e427d4219b2f5d55646c4e34f
Source noteuspto-grants-2010_09