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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 468413생성일: 2026년 10월 24일

Nitric Acid → Ethyl 5-methyl-2,4-dinitrobenzoate

https://huagongshe.com/ko/reaction/468413

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물Sulfuric AcidHCID 1118—
반응물3-Methylbenzoic acidHCID 7418—
반응물Thionyl ChlorideHCID 24386—
반응물5-Methyl-2,4-dinitrobenzoic acidHCID 3671900—
반응물3-Methyl-2,6-dinitrobenzoic acidHCID 54096940—
용매EthanolHCID 702—
생성물Ethyl 5-methyl-2,4-dinitrobenzoateHCID 1518463225.4%

반응 단계

To a mixture of HNO3 (95%, 80 mL) and H2SO4 (98%, 80 mL) was slowly added 3-methylbenzic acid (50 g, 0.37 mol) at 0° C. After addition, the mixture was stirred below 30° C. for 1.5 hours. The mixture was then poured into ice-water and stirred for 15 min. The precipitate solid was filtered and washed with water to give a mixture of 3-methyl-2,6-dinitro-benzoic acid and 5-methyl-2,4-dinitrobenzoic acid (70 g, 84%). To a solution of this mixture (70 g, 0.31 mol) in EtOH (150 mL) was added dropwise SOCl2 (54 g, 0.45 mol). The mixture was heated at reflux for 2 h before being concentrated to dryness under reduced pressure. The residue was partitioned between EtOAc (100 mL) and aq. Na2CO3 (10%, 120 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4, and concentrated to dryness to obtain ethyl 5-methyl-2,4-dinitrobenzoate (20 g), which was placed aside. The aqueous layer was acidified by HCl to pH 2˜3 and the precipitated solid was filtered, washed with water, and dried in air to give 3-methyl-2,6-dinitrobenzoic acid (39 g, 47%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623905B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-a859ea772534485cbec82f374c0e932f
출처 메모uspto-grants-2014_01