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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68466생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물p-FluoronitrobenzeneHCID 9590—
반응물Sodium hydrideHCID 24758—
반응물3-MorpholinoneHCID 66953—
반응물HCID 178418361HCID 178418361—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4-(4-Nitrophenyl)-morpholin-3-ONHCID 1144737517.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822458B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-965ed1c7175948cc9794bb3962fe9f51
출처 메모uspto-grants-2014_09