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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36922Erstellt: 24. Oktober 2026

Oxalyl chloride → 2,4-Difluorophenylacetyl chloride

https://huagongshe.com/de/reaction/36922

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt2,4-Difluorophenylacetic acidHCID 123581—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,4-Difluorophenylacetyl chlorideHCID 15231606—

Reaktionsschritte

To a mixture of 2,4-difluorophenylacetic acid (206 mg), DMF (1 drop) and tetrahydrofuran (4 ml) was added oxalyl chloride (0.13 ml) dropwise. The resulting mixture was stirred at room temperature for 1 hour and the solvent was then distilled off to give 2,4-difluorophenylacetyl chloride. This chloride was dissolved in dichloromethane (5 ml) followed by addition of 3-amino-4-(2-chlorophenyl)-7,8-dihydro-6H-cyclopenta[g]quinoline (294 mg) and N,N-dimethylaniline (0.13 ml). The mixture was further stirred at room temperature for 3 hours, after which it was washed with water, saturated aqueous solution of NaHCO3 and water in the order mentioned and dried (over MgSO4). The solvent was then distilled off to give 4-(2-chlorophenyl)-3-(2,4-difluorophenylacetylamino)-7,8-dihydro-6H-cyclopenta(g)quinoline as oil. This oil was crystallized from isopropyl ether (yield 342 mg, 76.3%). Recrystallization from ethanol gave colorless prisms, mp. 179°-180° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05418239
Quelldatensatzuspto-grants-1995_05
ORD IDord-7136b0aec2a94decbecda8f435272e8f
Quellennotizuspto-grants-1995_05