戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 68466作成日:2026年10月25日

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

https://huagongshe.com/reaction/68466

反応式

関与物質

役割名称HCID仕込み量
反応物p-FluoronitrobenzeneHCID 9590—
反応物Sodium hydrideHCID 24758—
反応物3-MorpholinoneHCID 66953—
反応物HCID 178418361HCID 178418361—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物4-(4-Nitrophenyl)-morpholin-3-ONHCID 1144737517.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822458B2
出典データセットuspto-grants-2014_09
ORD IDord-965ed1c7175948cc9794bb3962fe9f51
出典メモuspto-grants-2014_09