Reaktion #69356

Reaktionsgleichung

4-fluoronitrobenzene

sodium hydride

morpholin-3-one

hydrogen

→

4-(4-Morpholin-3-onyl)nitrobenzene

Ausbeute 17.6%

Lösungsmittel

N-methylpyrrolidone

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.DISTILLATIONAt 12 mbar and 76° C., 1.7 l of the liquid volume are then distilled off
2. 2
   workup.ADDITIONthe residue is poured into 2 l of water
3. 3
   Extraktionthis mixture is extracted twice with in each case 1 l of ethyl acetate
4. 4
   WaschenAfter washing of the combined organic phases with water
5. 5
   Trocknenthe mixture is dried over sodium sulphate
6. 6
   workup.DISTILLATIONthe solvent is distilled off under reduced pressure
7. 7
   SonstigePurification
8. 8
   Sonstigehexane/ethyl acetate (1:1) and subsequent crystallization from ethyl acetate

Vorschrift

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.

Quelle