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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29660생성일: 2026년 10월 23일

Triethylamine → 2-(4-Tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl ester

https://huagongshe.com/ko/reaction/29660

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-tert-Butylbenzoyl chlorideHCID 74372—
반응물Methyl 4-nitroanthranilateHCID 596476—
용매DichloromethaneHCID 6344—
용매Sodium chloride; waterHCID 57417360—
생성물2-(4-Tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl esterHCID 6919452960%

반응 단계

To a solution of 4-nitro-anthranilic acid methyl ester (1.500 g, 7.4 mmol) in CH2Cl2 (200 mL) was added triethylamine (8 mL) and 4-tert-butyl benzoyl chloride and the reaction was stirred overnight at rt. It was then poured into brine, extracted with ethyl acetate, dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography using ethyl acetate/hexanes (20/80) to afford 2-(4-tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl ester (1.841 g, 60%) as a yellow solid. mp=146.0-148.4° C.; mass spectrum (−ES, M−H) in/z 355. 1H NMR (400 MHz, DMSO-d6); δ 11.60 (bs, 1H), 9.35 (d, 1H), 8.20 (d, 1H), 8.02 (dd, 1H), 7.90 (d, 2H), 7.64 (d, 2H), 3.95 (s, 3H), 1.36 (s, 9H). Elemental analysis: Calcd. for C19H20N2O5: C, 64.04; H, 5.66; N, 7.86, Found: C, 64.04; H, 5.79; N, 7.76.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420083B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-72ec1c9158684e528be265558f7462da
출처 메모uspto-grants-2008_09