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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1870931생성일: 2026년 10월 27일

Ammonia → 2-Carbamoyl-3-nitrobenzoic acid

https://huagongshe.com/reaction/1870931

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물3-Nitrophthalic anhydrideHCID 21631—
반응물Ammonium 2-(aminocarbonyl)benzoateHCID 3083555—
생성물2-Carbamoyl-3-nitrobenzoic acidHCID 437547—

반응 조건

온도300 °C

반응 단계

3-Nitrophthalic anhydride (10.0 g, 50 mmol) was added in portions over 20 minutes to concentrated aqueous ammonia solution (15 ml), and the mixture was stirred at 300° C. for a further 30 minutes. The crystalline mass of ammonium phthalamate, deposited upon cooling the pale yellow solution, was collected and redissolved in a minimum amount of warm water. Concentrated hydrochloric acid (4.5 ml) was added dropwise, with stirring, and the resulting paste was washed with water, and dried in vacuo to give 3-nitrophthalamic acid as a fine white powder. (9.01 g, 83%), m.p. 217° C. Found: C, 45.76; H, 2.79; N, 13.21. C8H6N2O5 requires C, 45.71; H, 2.86; N, 13.33%; vmax /cm-1 3466.52, 3321.84, 1668.64, 1604.98, and 1525.89; δH (d6 -DMSO, 200 MHz) 7.75 (1H, br s, CONH), 7.8 (1H, t, Ar-5H), 8.16 (1H, brs, CONH), 8.2 (1H, d, Ar-6H), 8.3 (1H, d, Ar-4H); δC (d6 -DMSO) 127.32, 130.06, 132.28, 133.49, 134.78, 147.71, 166.25, and 166.60; m/z (EI) 192 (M+ -1), 177, 149, 103, 75.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06100283
출처 데이터셋uspto-grants-2000_08
ORD IDord-8f68f01615034c159b981bb4c747971f
출처 메모uspto-grants-2000_08