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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1165476Erstellt: 26. Oktober 2026

Sodium hydride → 3-(3,4-Dimethoxyphenyl)-3-(4-nitrophenyl)-acrylic acid morpholide

https://huagongshe.com/reaction/1165476

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktPhosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl esterHCID 11207805—
Edukt(3,4-Dimethoxyphenyl)(4-nitrophenyl)methanoneHCID 13954267—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(3,4-Dimethoxyphenyl)-3-(4-nitrophenyl)-acrylic acid morpholideHCID 54164249624,4%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

10.3 g of sodium hydride with 20% paraffin oil (0.343 mol) were suspended in 350 ml of tetrahydrofuran while stirring, and 75 g of diethylphosphonoacetic acid morpholide (0.0283 mol) were added dropwise to the suspension over a period of 20 minutes while cooling with ice (internal temperature 25° C.). The mixture was allowed to react for an hour during which a clear solution was formed. 70 g (0.244 mol) of 3,4-dimethoxy-4'-nitrobenzophenone were added to this solution all at once, and the mixture was refluxed for 2 hour while stirring. The solution was then evaporated in vacuo in a rotary evaporator at 60° C., and the residue was dissolved in methylene chloride/water. The organic phase was washed with water, dried over sodium sulfate and evaporated in vacuo at 60° C. The residue was triturated with 300 ml of hot methanol. 70.4 g of the title compound were obtained in the form of a faintly beige powder (73% of theory), m.p. 149°-163° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04910200
Quelldatensatzuspto-grants-1990_03
ORD IDord-fe8546b3839e4e0cb86c63b4eb23a4e9
Quellennotizuspto-grants-1990_03