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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68466Erstellt: 23. Oktober 2026

p-Fluoronitrobenzene → 4-(4-Nitrophenyl)-morpholin-3-ON

https://huagongshe.com/de/reaction/68466

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-FluoronitrobenzeneHCID 9590—
EduktSodium hydrideHCID 24758—
Edukt3-MorpholinoneHCID 66953—
EduktHCID 178418361HCID 178418361—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt4-(4-Nitrophenyl)-morpholin-3-ONHCID 1144737517,6%

Reaktionsschritte

2 mol (202 g) of morpholin-3-one (E. Pfeil, U. Harder, Angew. Chem. 79, 1967, 188) are dissolved in 2 l of N-methylpyrrolidone (NMP). Over a period of 2 h, 88 g (2.2 mol) of sodium hydride (60% in paraffin) are then added a little at a time. After the evolution of hydrogen has ceased, 282 g (2 mol) of 4-fluoronitrobenzene are added dropwise with cooling at room temperature, over a period of 1 h, and the reaction mixture is then stirred overnight. At 12 mbar and 76° C., 1.7 l of the liquid volume are then distilled off, the residue is poured into 2 l of water and this mixture is extracted twice with in each case 1 l of ethyl acetate. After washing of the combined organic phases with water, the mixture is dried over sodium sulphate and the solvent is distilled off under reduced pressure. Purification is carried out by silica gel chromatography using hexane/ethyl acetate (1:1) and subsequent crystallization from ethyl acetate. This gives 78 g of product as a colourless to brownish solid, in a yield of 17.6% of theory.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822458B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-965ed1c7175948cc9794bb3962fe9f51
Quellennotizuspto-grants-2014_09