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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34745Erstellt: 24. Oktober 2026

3-Bromoquinoline → 3-(Dimethoxyacetyl)quinoline

https://huagongshe.com/de/reaction/34745

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-BromoquinolineHCID 21413—
EduktN-(dimethoxyacetyl)morpholineHCID 21298597—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(Dimethoxyacetyl)quinolineHCID 14276934—

Reaktionsschritte

3-Bromoquinoline (3.29 ml., 0.032 mol) was dissolved in 300 ml. THF and cooled to -78°. n-Butyllithium (13.6 ml. of 2.5M in hexane, 0.034 ml.) was added slowly and the mixture stirred 15 minutes at -75° to -78°. N-(Dimethoxyacetyl)morpholine (5.98 g., 0.032 mol) in 10 ml. THF was then added and stirring continued for 1.75 hours at the same temperature. The reaction was then quenched into 300 ml. saturated NH4Cl. The aqueous layer was separated and extracted 4×100 ml. ether. The organic layers were combined, dried over MgSO4, stripped to yield title product, 7.0 g., bp 120°-123°/0.125 torr.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04762921
Quelldatensatzuspto-grants-1988_08
ORD IDord-97c01dee82af4b81ba08bf372d90172a
Quellennotizuspto-grants-1988_08