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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1260908Erstellt: 25. Oktober 2026

Formaldehyde → HCID 68871722, Verbindung

https://huagongshe.com/reaction/1260908

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktDiethyl OxalateHCID 7268—
EduktPotassium CarbonateHCID 11430—
EduktSodium hydrideHCID 24758—
EduktEthyl 3,4-dichlorophenylacetateHCID 2737422—
LösungsmittelEthanolHCID 702—
LösungsmittelM-XyleneHCID 7929—
ProduktHCID 68871722HCID 6887172271%

Reaktionsschritte

To a solution of sodium hydride (60% in oil, 6.56 g) in m-xylene (100 mL) was slowly added ethanol (15.7 mL) at 0° C. and then diethyl oxalate (32.0 g) was added. Furthermore, a solution of ethyl 3,4-dichlorophenylacetate (51.0 g) in m-xylene (30 mL) was added at 0° C., and the mixture was stirred at room temperature for 14 hr. To the reaction mixture was added 37% aqueous formalin solution (140 mL) at room temperature, and the mixture was stirred at room temperature for 1 hr. Furthermore, potassium carbonate (115 g) was added at room temperature, and the mixture was stirred at room temperature for 1 hr. The insoluble material was filtered off, and the filtrate was partitioned between ethyl acetate (500 mL) and water (500 mL). The organic layer was separated, washed with brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent; 5% ethyl acetate/hexane) to give crude ethyl 2-(3,4-dichlorophenyl)acrylate (38.1 g, 44%) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08470816B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-11372bb424614079a4c3aaf91b641a85
Quellennotizuspto-grants-2013_06