HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25284Erstellt: 23. Oktober 2026
Toluene → [3-(4-Trifluoromethylphenyl)phenyl]cyclopentyl sulfide
https://huagongshe.com/de/reaction/25284
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 4-(Trifluoromethyl)phenylboronic acid | HCID 2734389 | — |
| Edukt | 1-Bromo-3-(cyclopentylthio)benzene | HCID 22170879 | — |
| Katalysator | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | [3-(4-Trifluoromethylphenyl)phenyl]cyclopentyl sulfide | HCID 17808972 | 78% |
Reaktionsschritte
1.0 g (5.2 mol) of 4-trifluoromethylphenyl boronic acid, 1.4 g (5.4 mmol) of 3-bromophenyl cyclopentyl sulfide, 1.6 g (15.0 mmol) of sodium carbonate and 0.8 g (0.7 mmol) of tetrakis(triphenylphosphine) palladium were added to a solvent mixture of 50 ml of toluene, 25 ml of ethanol and 25 ml of water and refluxed under heating and stirring for 2 hours. The resulting reaction mixture was poured into ice-cold water and extracted with toluene. The toluene layer was washed with water twice and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 1.3 g of [3-(4-trifluoromethylphenyl)phenyl] cyclopentyl sulfide (yield 78.0%) as a colorless liquid (nD20 1.5732).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06858639B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-04e4602c366d45ddbdb1050a3e7d0fb4 |
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| Quellennotiz | uspto-grants-2005_02 |
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