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HRID 40182Erstellt: 23. Oktober 2026

Tetrahydrofuran → Ethyl 3-(7-methoxyquinolin-4-yl)propanoate

https://huagongshe.com/de/reaction/40182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Edukt4-Chloro-7-methoxyquinolineHCID 10607829—
EduktHCID 178471816HCID 178471816—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelAmmonium HydroxideHCID 14923—
ProduktEthyl 3-(7-methoxyquinolin-4-yl)propanoateHCID 67503802—

Reaktionsschritte

4-chloro-7-methoxyquinoline (0.35 g, 2 mmol), tri-t-butylphosphonium tetrafluoroborate (0.05 g, 0.2 mmol), and tris(dibenzylideneacetone)dipalladium (0) (0.08 g, 0.09 mmol) were combined. The reaction vessel was purged and flushed with nitrogen three times, followed by addition of 3-ethoxy-3-oxopropylzinc bromide in THF (10 mL, 5 mmol, 0.5 M). The reaction mixture was microwaved at 150° C. for 60 minutes. Upon completion, ammonium hydroxide (10 mL) was added. After 30 minutes the mixture was filtered and the filtrate was partitioned between water and ethyl acetate. Extracted with ethyl acetate (3×20 mL). The organic layers were combined, washed with brine, dried over magnesium sulfate, and concentrated. Purified by MPLC with a gradient of 20 to 50% EtOAc in CH2Cl2. (ESI, pos. ion) m/z: 354.1 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524900B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-2749dc371527437e9924f4eb2acea80b
Quellennotizuspto-grants-2013_09