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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 491631생성일: 2026년 10월 26일

4-Chloro-2-nitroaniline → 3-(4-amino-3-nitro-phenoxy)-N-methyl-benzamide

https://huagongshe.com/reaction/491631

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-2-nitroanilineHCID 6979—
반응물Sodium hydrideHCID 24758—
반응물3-hydroxy-N-methylbenzamideHCID 353710—
용매DimethylformamideHCID 6228—
생성물3-(4-amino-3-nitro-phenoxy)-N-methyl-benzamideHCID 69017532—

반응 조건

온도80 °C

반응 단계

To a solution of 3-hydroxy-N-methyl-benzamide (Step A, 700 mg, 4.6 mmol, 1.0 eq.) in anhydrous DMF (10 mL) was added NaH (200 mg, 5.1 mmol, 1.1 eq.). The reaction was stirred for 10 min. at RT after which 4-chloro-2-nitro-phenylamine (2.0 g, 11.6 mmol, 2.5 eq.) was added. The resulting mixture was heated to 80° C. for 4 h. The reaction was quenched with NaHCO3 (aq.), diluted with CH2Cl2 (50 mL), and washed with 1 N NaOH (25 mL). The organic layer was dried over MgSO4, filtered and concentrated. The crude was further purified by column chromatography (0-100% EtOAc in hexanes) to give pure 3-(4-amino-3-nitro-phenoxy)-N-methyl-benzamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07531553B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-d9c24b3c6a0d486cb91bee5fb968016a
출처 메모uspto-grants-2009_05