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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349467생성일: 2026년 10월 26일

p-Toluenesulfonic acid → 4-methoxy-3-[(N-chloro-benzimidoyl)-amino]-benzoic acid methyl ester

https://huagongshe.com/reaction/349467

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참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물BenzonitrileHCID 7505—
반응물Sodium BicarbonateHCID 516892—
반응물Methyl 3-Amino-4-methoxybenzoateHCID 2734814—
반응물Sodium HypochloriteHCID 23665760—
생성물4-methoxy-3-[(N-chloro-benzimidoyl)-amino]-benzoic acid methyl esterHCID 6911957488%

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온도180 °C

반응 단계

Anhydrous p-toluene sulfonic acid (41.99 g, 220.8 mmol) was melted at 120° C. and 3-amino-4-methoxy benzoic acid methyl ester (20 g, 110.38 mmol) obtained in step 1 and benzonitrile (22.77 g, 220.8 mmol) were added thereto and stirred at 180° C. for 5 hours. The resulting solution was cooled to room temperature and the reaction was stopped by adding NaHCO3 thereto. The resulting mixture was extracted with ethyl acetate, the extract was dried over MgSO4 and concentrated under a reduced pressure. The concentrate was dissolved in 50% methanol and 5% NaOCl (56 Ml, 37.65 mmol) was added dropwise thereto. After 5 min, the resulting mixture was extracted with ethyl acetate, the extract was dried over MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent—MeOH/CDCl3=5:95, Merck, Silicagel 60) to obtain the title compound (31 g, 25.10 mmol) in a yield of 88%;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179832B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-355faa56b66949f6b215a49bf9a90720
출처 메모uspto-grants-2007_02