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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194680Generated: October 27, 2026

Thiophenol → 1-(2-Fluorophenyl)-2-(phenylthio)ethanone

https://huagongshe.com/reaction/2194680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-2'-fluoroacetophenoneHCID 2737449—
SolventEthanolHCID 702—
Product1-(2-Fluorophenyl)-2-(phenylthio)ethanoneHCID 4341334564%

Reaction Steps

To a suspension of 2-bromo-1-(2-fluorophenyl)ethanone (3.0 g) and potassium carbonate (2.0 g) in ethanol (30 mL) was added dropwise thiophenol (1.4 mL) at 0° C. The mixture was stirred at room temperature for 8 hr, insoluble materials were filtered off, and the filtrate was concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution, water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=15:1) to give the title compound as a pale-yellow solid (yield 2.2 g, yield 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334301B2
Source datasetuspto-grants-2012_12
ORD IDord-58361aa1d8804dfbb47fd11e1298072f
Source noteuspto-grants-2012_12