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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 477330Erstellt: 24. Oktober 2026

2-Methoxy-1-phenylethanone → Ethyl 2-dimethylamino-5-methoxy-6-oxo-6-phenyl-2,4-hexadienoate

https://huagongshe.com/de/reaction/477330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methoxy-1-phenylethanoneHCID 77698—
EduktSodium ethoxideHCID 2723922—
EduktEthyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino2,4-hexadienoateHCID 44325574—
EduktN-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743575—
LösungsmittelEthanolHCID 702—
ProduktEthyl 2-dimethylamino-5-methoxy-6-oxo-6-phenyl-2,4-hexadienoateHCID 53661101—

Reaktionsschritte

The procedure is as in Example 4 for the preparation of ethyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino2,4-hexadienoate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (11.4 g), a 2M ethanolic solution of sodium ethylate (20 cc) and α-methoxyacetophenone (6 g) in ethanol (50 cc). After purification by chromatography on a silica column with a mixture of dicholoromethane and ethyl acetate (50:50 by volume) as eluent, ethyl 2-dimethylamino-5-methoxy-6-oxo-6-phenyl-2,4-hexadienoate (8.1 g) is obtained, and is used in the crude state in the subsequent syntheses.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04886835
Quelldatensatzuspto-grants-1989_12
ORD IDord-6e6464c9218943b8abb6cc76a80a7f64
Quellennotizuspto-grants-1989_12