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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 361728생성일: 2026년 10월 26일

Benzenesulfonamide, 3-nitro- → Benzenesulfonamide, 3-amino-

https://huagongshe.com/reaction/361728

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonamide, 3-nitro-HCID 67138—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물Benzenesulfonamide, 3-amino-HCID 7377100.2%

반응 단계

A solution of 1.5 g (7.42 mmol) of 3-nitrobenzenesulfonamide in 50 ml of EtOH containing 150 mg of 10% palladium on carbon was placed on a Parr hydrogenator under H2 for 1 h. The reaction was filtered through a pad of celite washing with EtOH, and the filtrate was concentrated in vacuo to give 1.28 g (100%) of 3-aminobenzenesulfonamide which was used immediately in the next reaction. The title compound was prepared as in example 21 from 3-aminobenzenesulfonamide using intermediate C. Recrystallization from MeOH/Et2O provided 1.46 g (67%) of title compound as an off-white solid: mp 240°-242° C.; 1H NMR (D2O, 300 MHz) δ 7.86 (d, 1 H, J=8.1 Hz), 7.75 (s, 1 H), 7.63 (t, 1 H, J=8.1 Hz), 7.51 (d, 1 H, J=8.1 Hz), 2.30 (s, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05866612
출처 데이터셋uspto-grants-1999_02
ORD IDord-fe4f2101ef084b0185c7e95b7efe8dfd
출처 메모uspto-grants-1999_02