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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280250생성일: 2026년 10월 24일

P-Anisidine → 6-Chloro-2-(4-methoxyanilino)-3-nitrobenzoic acid

https://huagongshe.com/ko/reaction/280250

반응식

참여 물질

역할이름HCID투입량
반응물P-AnisidineHCID 7732—
반응물2,6-Dichloro-3-nitrobenzoic acidHCID 350623—
생성물6-Chloro-2-(4-methoxyanilino)-3-nitrobenzoic acidHCID 2778012—

반응 단계

To 74 g (0.60 mol) of p-anisidine, stirred mechanically at 75 degrees, was added 35.4 g (0.15 mol) of 2,6-dichloro-3-nitrobenzoic acid [Lehmstedt and Schrader, Berichte 70B, 1526 (1937)]in small portions over one-half hour. The mixture was heated at 75 degrees for 24 hours, with stirring during the first two hours. The reaction mixture was cooled, the solid mass shattered, and triturated in a mechanical blender with 300 ml of 2.4N hydrochloric acid. The solid was collected, washed with 3N hydrochloric acid, stirred in 400 ml of 0.5N sodium carbonate, and filtered. The filtrate, diluted with 250 ml of water, was gradually acidified with 4N hydrochloric acid. The precipitate was collected, washed with water, and dried to 38.5 g (79%) of the red title compound, mp 205-213 degrees. A purified sample, from toluene, melts at 212-215 degrees.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04588730
출처 데이터셋uspto-grants-1986_05
ORD IDord-0167cc214a8147138fc621d21f7a3ecc
출처 메모uspto-grants-1986_05