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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29673생성일: 2026년 10월 24일

Triethylamine → 4-Nitro-2-(4-trifluoromethoxy-benzoylamino)-benzoic acid methyl ester

https://huagongshe.com/ko/reaction/29673

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(Trifluoromethoxy)benzoyl ChlorideHCID 142110—
반응물Methyl 4-nitroanthranilateHCID 596476—
용매DichloromethaneHCID 6344—
생성물4-Nitro-2-(4-trifluoromethoxy-benzoylamino)-benzoic acid methyl esterHCID 6920543570%

반응 단계

To a solution of 2-amino-4-nitro-benzoic acid methyl ester (5.00 g, 25.5 mmol) in methylene chloride (75 mL) was added triethylamine (4.13 g, 40.8 mmol) followed by 4-trifluoromethoxy-benzoyl chloride (6.87 g, 30.6 mmol). This mixture was allowed to stir overnight at ambient temperature. The mixture was filtered, partitioned against brine, the layers were separated, and the aqueous layer was extracted with one portion of ethyl acetate. The organics were combined, dried over MgSO4, filtered and concentrated under reduced pressure. The crude material was recrystallized from ethyl acetate (250 mL) to give 4-nitro-2-(4-trifluoromethoxy-benzoylamino)-benzoic acid methyl ester (6.83 g, 70%) as pale-yellow crystals. 1H NMR (500 MHz, DMSO-d6); δ 11.53 (s, 1H), 9.20 (d, 1H), 8.19 (d, 1H), 8.10 (d, 2H), 8.07 (dd, 1H), 7.63 (d, 2H), 3.91 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420083B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-4a04ac522eff4b92bea5eced178dcb90
출처 메모uspto-grants-2008_09