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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16023Erstellt: 23. Oktober 2026

Ammonium Chloride → 1-(Quinolin-6-yl)ethan-1-one

https://huagongshe.com/de/reaction/16023

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktN-Methoxy-N-methylquinoline-6-carboxamideHCID 55211172—
EduktHCID 178418689HCID 178418689—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(Quinolin-6-yl)ethan-1-oneHCID 25855997,1%

Reaktionsschritte

To a solution of quinoline-6-carboxylic acid methoxy-methyl-amide (11.97 g, 55.35 mmol) in anhydrous THF (200 mL) was added MeMgBr (1.5 M in THF, 55 mL, 83 mmol) at 0° C. under nitrogen. The reaction was allowed to warm to ambient temperature over 16 hours. Sat. NH4Cl (20 mL) was added to quench the reaction. The reaction solution was then extracted with EtOAc (3×50 mL). The combined organics were dried over Na2SO4, filtered, and concentrated to give 1-quinolin-6-yl-ethanone (9.2 g, 97% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732604B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-1b533ba8a3a34f338769c7d82baef3e5
Quellennotizuspto-grants-2010_06