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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2108876Erstellt: 26. Oktober 2026

Chloroform → 4-[(5-Bromopentyl)sulfanyl]-7-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/2108876

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
Edukt1,5-DibromopentaneHCID 8100—
EduktPotassium CarbonateHCID 11430—
EduktHCID 178506078HCID 178506078—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
Produkt4-[(5-Bromopentyl)sulfanyl]-7-(trifluoromethyl)quinolineHCID 1797581572%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

7-Trifluoromethyl-4-quinoline-thiol (5 g, 21.8 mmol), 1,5-dibromopentane (23.7 g, 98.1 mmol) and CHCl3 (60 mL) were charged in a 250 ml round-bottomed flask equipped with a magnetic stirrer. TBABr (0.7 g, 2.2 mmol) and water (40 mL) were added and the reaction mixture was stirred for 48 h at 20° C. The reaction mixture was poured in 100 mL of H2O with K2CO3 (3.0 g, 21.8 mmol) and extracted with CH2Cl2 (400 mL). The organic layer was washed with water (30 mL), brine (2×30 mL), dried over MgSO4, filtered and evaporated at 30° C. to dryness. The crude compound was purified by column chromatography (SiO2:CH2Cl2:MeOH=99.5:0.5 to 98:2) to give after evaporation 4-(5-bromopentylthio)-7-(trifluoromethyl)quinoline 25 (5.9 g, 72% yield) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07514432B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-5ddb69884b0e43a7837a8afe289ae646
Quellennotizuspto-grants-2009_04