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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-2'-fluoroacetophenone | HCID 2737449 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(2-Fluorophenyl)-2-(phenylthio)ethanone | HCID 43413345 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334301B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-58361aa1d8804dfbb47fd11e1298072f |
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| Source note | uspto-grants-2012_12 |
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