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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11562생성일: 2026년 10월 23일

(4-Nitrophenyl)acetic acid → 1-(4-Morpholinyl)-2-(4-nitrophenyl)ethanone

https://huagongshe.com/ko/reaction/11562

반응식

참여 물질

역할이름HCID투입량
반응물(4-Nitrophenyl)acetic acidHCID 4661—
반응물MorpholineHCID 8083—
반응물Sodium BicarbonateHCID 516892—
용매TetrahydrofuranHCID 8028—
생성물1-(4-Morpholinyl)-2-(4-nitrophenyl)ethanoneHCID 5170165—

반응 조건

온도35 °C

반응 단계

A room temperature solution of 1.8839 gms. (4-Nitro-phenyl)-acetic acid in tetrahydrofuran (5 mL) is treated with 1.8069 gms. 1′,1′-carbonyl-diimidizole. The reaction mixture is stirred for 1 h. The reaction mixture is then treated with 1.0 mL morpholine. The reaction is heated overnight at 35° C. The reaction is then allowed to cool to room temperature, and is made basic with the addition of saturated aqueous sodium bicarbonate. The resulting mixture is extracted with ethyl acetate. The aqueous layer is re-extracted four more times with ethyl acetate. The combined organics are evaporated to dryness in vacuo. The crude product residue is then chromatographed by flash silica gel chromatography using 60% ethyl acetate in hexanes as the eluant. Following evaporation of solvent, 1-morpholin-4-yl-2-(4-nitro-phenyl)-ethanone is isolated as a white solid in the amount of 1.4009 gms.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098236B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f62c3c18b80740c0b6b9fd0839671267
출처 메모uspto-grants-2006_08