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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1945376생성일: 2026년 10월 27일

Trichlorophenoxyacetic acid → 3-[2-(2,4,5-Trichloro-phenoxy)-acetylamino]-benzoic acid methyl ester

https://huagongshe.com/reaction/1945376

반응식

참여 물질

역할이름HCID투입량
반응물Trichlorophenoxyacetic acidHCID 1480—
반응물Benzoic acid, 3-amino-, methyl esterHCID 78274—
반응물PyBOPHCID 2724699—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
생성물3-[2-(2,4,5-Trichloro-phenoxy)-acetylamino]-benzoic acid methyl esterHCID 2481100185.6%

반응 단계

The mixture of (2,4,5-trichloro-phenoxyacetic acid (127.8 mg, 0.5 mmol), 3-aminobenzoic acid methyl ester (151.2 mg, 1.0 mmol), 4-dimethylaminopyridine (122.2 mg, 1.0 mmol) and benzotriazole-1-yl-oxy-tris-pyrrolidino-phosphonium hexafluorophosphate (pybop) (520.3 g, 1.0 mmol) in DMF (5.0 mL) was stirred overnight and then partitioned between ethyl acetate and 10% HCl. The organic phase was washed with brine, dried (MgSO4 anh), and concentrated. The residue was purified by silica gel flash column chromatography (n-Hexane:Ethyl acetate:MeOH=6:3:1) to give 3-[2-(2,4,5-trichloro-phenoxy)-acetylamino]-benzoic acid methyl ester as a white solid (166.4 mg, 85.6% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08394799B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-abdd9bc9d0c347d5a931bf1da08883e2
출처 메모uspto-grants-2013_03