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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 580604Erstellt: 24. Oktober 2026

Water → 4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholide

https://huagongshe.com/de/reaction/580604

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
EduktPhosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl esterHCID 11207805—
EduktHCID 13373314HCID 13373314—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholideHCID 54521919—

Reaktionsschritte

A solution of 5.3 g (0.02 mol) of diethylphosphonoacetic acid morpholide in 100 ml of dry tetrahydrofuran was slowly added dropwise, while stirring, to a suspension of 1 g of sodium hydride (0.02 mol, 50% in oil) in 50 ml of dry tetrahydrofuran. Slight heating and strong foaming occurred. After all had been added, the mixture was stirred for 10 minutes more. A solution of 3 g (0.01 mol) of 4-amino-3,4',5-trichlorobenzophenone in 20 ml of dry tetrahydrofuran was added dropwise to the resulting clear solution, and the mixture was heated for 16 hours at reflux temperature. After cooling, the solution was poured into water, and the aqueous mixture was extracted exhaustively with methylene chloride. The methylene chloride phase was dried with sodium sulfate and evaporated by evaporation in vacuo. The residue was crystallized from isopropanol/petroleum ether. The colorless crystals thus obtained, melting point 150°-155° C., contained the cis/trans isomers in a ratio of 1:3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04753934
Quelldatensatzuspto-grants-1988_06
ORD IDord-d3a7eb78bd444d0fb967eeb28ced0d84
Quellennotizuspto-grants-1988_06