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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 477331Erstellt: 23. Oktober 2026

Sodium ethoxide → Diethyl 2-dimethylamino-5-(4-methylbenzylthio)-2,4-hexadienedioate

https://huagongshe.com/de/reaction/477331

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ethoxideHCID 2723922—
EduktEthyl (4-methylbenzylthio)acetateHCID 4107274—
EduktN-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743575—
EduktDiethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioateHCID 86743580—
LösungsmittelEthanolHCID 702—
ProduktDiethyl 2-dimethylamino-5-(4-methylbenzylthio)-2,4-hexadienedioateHCID 5384798766,5%

Reaktionsschritte

The procedure is as in Example 2 for the preparation of diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (5.7 g), a 2M ethanolic solution of sodium ethylate (10 cc) and ethyl (4-methylbenzylthio)acetate (4.5 g) in ethanol (50 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (50:50 by volume) as eluent, diethyl 2-dimethylamino-5-(4-methylbenzylthio)-2,4-hexadienedioate (5 g) is obtained in the form of a yellow oil, 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-12abb86c430a49e490d5e491c3c8d3c4
Quellennotizuspto-grants-1989_12