Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1817782Erstellt: 24. Oktober 2026

Ammonia → 4-(4-Nitrophenyl)-morpholin-3-ON

https://huagongshe.com/de/reaction/1817782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktNitric AcidHCID 944—
EduktSulfuric AcidHCID 1118—
Edukt4-Phenylmorpholin-3-ONHCID 5153080—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
Produkt4-(4-Nitrophenyl)-morpholin-3-ONHCID 11447375—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

In a 2-liter flask, 177 g (1.0 mol) of 4-phenyl-3-morpholinone (VIII) are introduced at internal temperature 10° C. in 4 portions into 728 g (7.4 equivalents) of concentrated sulphuric acid. The mixture is then heated to 25° C. and stirred at this temperature for 30 minutes. The solution is cooled to −5° C. and admixed within one hour with 101.8 g (1.05 equivalents) of 65% nitric acid. The mixture is stirred at −5° C. for one hour. 1300 ml of demineralized water are metered into this solution at 10° C. Subsequently, a pH of 7.4 is established, likewise at 10° C., with 25% aqueous ammonia solution. The suspension is admixed with 2000 g of acetone and heated to 40° C. In the course of this, the product goes into solution, so that the phases can be separated. 1500 g of acetone/water mixture are distilled off at standard pressure from the organic phase, in the course of which the product precipitates out. The suspension is cooled to 10° C. and stirred for a further 30 minutes, and the product is isolated. The moist product is washed with 320 g of cold acetone and dried at 50° C. under reduced pressure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07598378B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-2ae314a9b3a6465b960c704de259a8cf
Quellennotizuspto-grants-2009_10