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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 406482Erstellt: 24. Oktober 2026

Ethyl iodoacetate → (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester

https://huagongshe.com/de/reaction/406482

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl iodoacetateHCID 12183—
EduktSodium hydrideHCID 24758—
Edukt3,4-dihydroisoquinolin-1(2H)-oneHCID 150896—
LösungsmittelTolueneHCID 1140—
Produkt(1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl esterHCID 59764846—

Reaktionsschritte

To a solution of 3,4-dihydro-2H-isoquinolin-1-one (0.250 g, 1.70 mmol) in toluene (5 mL) was added sodium hydride (60% in mineral oil, 0.049 g, 2.04 mmol) and the resulting suspension was heated at about reflux for about 1 h. The reaction mixture was cooled at room temperature and ethyl 2-iodoacetate (0.364 g, 1.70 mmol) was added dropwise and the mixture was again heated at about reflux for about 12 h. The reaction mixture was cooled at room temperature and filtered, rinsed with toluene. The filtrate was concentrated in vacuo to provide (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester as a peach oil (0.336 g, 1.44 mmol). The crude material was used in subsequent reactions without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754107B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-1d1de92b70de414f8fecb0ebfe936e74
Quellennotizuspto-grants-2014_06