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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53654Erstellt: 25. Oktober 2026

1,2-Dichloroethane → Quinoline

https://huagongshe.com/reaction/53654

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktQuinaldic AcidHCID 7124—
Edukt1-HydroxybenzotriazoleHCID 75771—
LösungsmittelDimethylformamideHCID 6228—
ProduktQuinolineHCID 7047319,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A 100 ml RBF equipped with magnetic stir bar and N2 inlet was charged with 356 mg (2.06 mmol, 1 eq) 2-quinaldic acid in 10 ml dry DMF. The solution was cooled to 0° C. and 415 mg (3.07 mmol, 1.5 eq) HOBt was added followed by 415 mg EDC (2.16 mmol, 1.05 eq). The reaction was stirred 2 hours at 0° C. when 1.1 g (2.06 mmol, 1 eq) of free asparagine amine in 10 ml dry DMF was added. The reaction was stirred at 0° C. for 2 hours then room temperature overnight. The reaction was poured into sat. bicarb and extracted with 2×65 mL ethyl acetate. The combined organics were washed with 5% aq. citric acid, brine, dried and concentrated to 1.4 g crude foam. Purification by flash chromatography on silica gel (100% ethyl acetate) yielded 850 mg (61%) of quinoline adduct.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05620977
Quelldatensatzuspto-grants-1997_04
ORD IDord-2418f6fa7a6540388b5cd366afeeca75
Quellennotizuspto-grants-1997_04