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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 500451Erstellt: 25. Oktober 2026

2-Chloroquinoline → 2-Cyclopentylquinoline

https://huagongshe.com/reaction/500451

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-ChloroquinolineHCID 11928—
EduktHCID 178419650HCID 178419650—
Katalysator[1,2-Bis(diphenylphosphino)ethane]dichloronickel(II)HCID 2734542—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelAmmonium ChlorideHCID 25517—
Produkt2-CyclopentylquinolineHCID 21826432100,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 2-chloroquinoline (8.2 g, 50 mmol) and [1,2-bis(diphenylphosphino)-ethane]dichloronickel(II) (200 mg, 0.38 mmol) in diethyl ether (20 ml) cooled in a ice/methanol bath was added cyclopentylmagnesium bromide (2 M solution in diethyl ether; 25.5 ml, 51 mmol) over a period of 15 minutes. The resulting brown solution was then stirred for 30 minutes, the ice bath removed and the mixture stirred for a further 10 minutes. The reaction mixture was then re-cooled to 0° C. and a saturated ammonium chloride solution (40 ml) added slowly. The resulting reaction mixture was poured into a separating funnel and further diluted with diethyl ether (60 ml) and saturated ammonium chloride solution (60 ml). The organics were separated and the aqueous layer washed with diethyl ether (2×100 ml). The combined organics were dried (MgSO4), filtered and the solvent removed in vacuo to leave 2-cyclopentylquinoline (9.98 g, 50.4 mmol) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07772227B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-6ef299c453e641a5a40b6ddbf30a612a
Quellennotizuspto-grants-2010_08