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HRID 22139Erstellt: 24. Oktober 2026

Water → 2-Di-n-propylamino-8-(quinol-2-yl)-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/de/reaction/22139

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2-ChloroquinolineHCID 11928—
EduktMagnesiumHCID 5462224—
Edukt8-Bromo-2-dipropylamino-1,2,3,4-tetrahydronaphthaleneHCID 14529564—
Katalysator1,2-DibromoethaneHCID 7839—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Di-n-propylamino-8-(quinol-2-yl)-1,2,3,4-tetrahydronaphthaleneHCID 23373524181,9%

Reaktionsschritte

2-Di-n-propylamino-8-bromo-1,2,3,4-tetrahydronaphthalene (1 g, 3.22 mmol) was added to a refluxing mixture of magnesium turnings (120 mg, 4.9 mmol) in 50 ml THF. Formation of the Grignard reagent was initiated by addition of 0.2 ml 1,2-dibromoethane (0.002 mmol). After 1.5 hours, 220 mg (0.33 mmol) Ni[PPh3 ]2Cl2 in 10 ml of THF were added followed by 800 mg (4.89 mmol) of 2-chloroquinoline. The solution continued to reflux for 15 minutes after which it was cooled, poured into water, and extracted three times with methalene chloride. The extract was dried with sodium sulfate and concentrated to obtain 2.1 g of a black oil. The crude was purified by using two flash columns. The first was eluted with 1:1 hexanes:ether and the second with 20:1 methylene chloride:methanol. 130 mg of the title compound were collected as product. Following crystallization in ethanol and water, 66 mg of solid were recovered, m.p. 82° C. Analysis: Theory (.1/3 H2O): C, 82.37; H, 8.48; N, 7.68; Found: C, 82.33; H, 8.44; N, 7.73.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05426226
Quelldatensatzuspto-grants-1995_06
ORD IDord-e52d946ba6b940f2adfefdb638da511e
Quellennotizuspto-grants-1995_06