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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 477356Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/477356

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ethoxideHCID 2723922—
EduktEthyl (4-isopropylbenzylthio)acetateHCID 54329641—
EduktN-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743575—
EduktDiethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioateHCID 86743580—
LösungsmittelEthanolHCID 702—
ProduktDiethyl 2-dimethylamino-5-(4-isopropylbenzylthio)-2,4-hexadienedioateHCID 5412334262,2%

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 (10 g), a 2M ethanolic solution of sodium ethylate (21 cc) and ethyl (4-isopropylbenzylthio)acetate (8.8 g) in ethanol (100 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (80:20 by volume) as eluent, diethyl 2-dimethylamino-5-(4-isopropylbenzylthio)-2,4-hexadienedioate (8.8 g) is obtained in the form of an orange-coloured 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-7acbd417327b45359bef572d316fff10
Quellennotizuspto-grants-1989_12