Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 479602Erstellt: 26. Oktober 2026

Tetrahydrofuran → Ethyl 4-(4-benzyloxyphenyl)-2-cyano-3-phenylbutyrate

https://huagongshe.com/reaction/479602

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt4-Benzyloxybenzyl chlorideHCID 70042—
EduktEthyl benzylidenecyanoacetateHCID 74845—
LösungsmittelTolueneHCID 1140—
ProduktEthyl 4-(4-benzyloxyphenyl)-2-cyano-3-phenylbutyrateHCID 18772157—

Reaktionsschritte

835 mg of Mg are suspended in 5 ml of abs. THF. A solution of 2.0 g of 4-benzyloxybenzyl chloride in 5 ml of abs. tetrahydrofuran is subsequently added dropwise. When the addition is complete, the cloudy solution is stirred at room temperature for a further 1 hour, a solution of 1.73 g of ethyl 2-cyano-3-phenylacrylate in 10 ml of abs. toluene is subsequently added, and the mixture is refluxed for 16 hours. The solvent is removed, and conventional work-up gives ethyl 4-(4-benzyloxyphenyl)-2-cyano-3-phenylbutyrate (“AA”).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06645991B1
Quelldatensatzuspto-grants-2003_11
ORD IDord-63baf29a43f746389e4276ede39451d5
Quellennotizuspto-grants-2003_11