Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Fluoronitrobenzene | HCID 9590 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 3-Morpholinone | HCID 66953 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | 4-(4-Nitrophenyl)-morpholin-3-ON | HCID 11447375 | 17,6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822458B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-965ed1c7175948cc9794bb3962fe9f51 |
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| Quellennotiz | uspto-grants-2014_09 |
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