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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74146생성일: 2026년 10월 23일

4-Anilino-3-nitrobenzoic acid → 3-Amino-4-phenylamino-benzoic acid

https://huagongshe.com/ko/reaction/74146

반응식

참여 물질

역할이름HCID투입량
반응물4-Anilino-3-nitrobenzoic acidHCID 3824366—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물3-Amino-4-phenylamino-benzoic acidHCID 77382195.3%

반응 단계

A 3-neck flask was charged with 3-nitro-4-phenylaminobenzoic acid (see Synthesis Example 1-1) (1.67 g, 6.70 mmol), palladium/carbon (Pd:10%, 0.170 g), and tetrahydrofuran (34 mL), the atmosphere was replaced with hydrogen using three cycles of vacuum/hydrogen purge, and this was stirred at room temperature for 2.5 hours. After substituting in nitrogen, distilled water (20 mL) was added and this was stirred for 10 minutes, insoluble material was filtered off through a Celite layer (20 mm thickness), and this same layer was further washed with tetrahydrofuran (20 mL, 3 times). The filtrate and the wash solutions were combined, and the solvent was distilled off under reduced pressure. This was successively extracted with ethyl acetate (approx. 50 mL, 4 times), washed with distilled water (30 mL), and dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and further drying under reduced pressure yielded the title compound (1.45 g, 95.3% yield) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3f6cded859c546208933eab05023e6dc
출처 메모uspto-grants-2014_09