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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1639831생성일: 2026년 10월 27일

Hydrochloric Acid → 2-Iodo-3-nitrobenzoic acid

https://huagongshe.com/reaction/1639831

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물Potassium IodideHCID 4875—
반응물Potassium HydroxideHCID 14797—
반응물Methyl 2-acetamido-3-nitrobenzoateHCID 2782278—
반응물Sodium NitriteHCID 23668193—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물2-Iodo-3-nitrobenzoic acidHCID 22096672%

반응 조건

온도60 °C

반응 단계

A mixture of methyl 2-(acetylamino)-3-nitrobenzoate (4.19 g, 17.6 mmol) and potassium hydroxide (4.93 g, 88.0 mmol) in water (20 mL) was stirred at 60° C. overnight. The resulting solid was collected by filtration, washed with methanol, and is suspended in water (14 mL). Concentrated hydrochloric acid (7.3 mL, 88 mmol) was added to the suspension, and a solution of sodium nitrite (1.88 g, 27.3 mmol) in water (10 mL) was added at 0° C. over 1.5 hr. The reaction mixture was added to a solution of potassium iodide (4.53 g, 27.3 mmol) and iodine (3.73 g, 14.7 mmol) in dimethyl sulfoxide (130 mL) at 5° C. over 20 min. The resulting reaction mixture was stirred at 50° C. for 20 min, and extracted with ethyl acetate. The extract was washed with water, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was washed with hexane to give the title compound (3.71 g, yield 72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08110585B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-0783df7c8fab4e3980b65a77e067d3ac
출처 메모uspto-grants-2012_02