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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1823156Erstellt: 27. Oktober 2026

Toluene → [3-(4-Trifluoromethylphenyl)phenyl]cyclopentyl sulfide

https://huagongshe.com/reaction/1823156

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktSodium CarbonateHCID 10340—
Edukt4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Edukt1-Bromo-3-(cyclopentylthio)benzeneHCID 22170879—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt[3-(4-Trifluoromethylphenyl)phenyl]cyclopentyl sulfideHCID 1780897278%

Reaktionsschritte

1.0 g (5.2 mmol) 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). 1H-NMR data (300 MHz, CDCl3 solvent, δ value)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07037930B2
Quelldatensatzuspto-grants-2006_05
ORD IDord-8ad04b0a098a4d75bc2b47f4832fffbf
Quellennotizuspto-grants-2006_05