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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14291생성일: 2026년 10월 24일

Hydrochloric Acid → 3-Iodo-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/ko/reaction/14291

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium IodideHCID 4875—
반응물3-Amino-5-(methoxycarbonyl)benzoic acidHCID 13557643—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물3-Iodo-5-(methoxycarbonyl)benzoic acidHCID 1584039155.1%

반응 단계

To an ice-cold, stirred solution of 3-amino-5-(methoxycarbonyl)benzoic acid (5.19 g, 26.59 mmol) in a 2 N hydrochloric acid (156 mL) was added a solution of sodium nitrite (1.84 g, 26.67 mmol) in water (10.8 mL). This mixture was then added dropwise to an ice-cold, stirred solution of potassium iodide (8.84 g, 53.25 mmol) in water (26.2 mL). After stirring for 35 min, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with 5% aqueous sodium thiosulfate, and saturated sodium chloride, dried (sodium sulfate), and concentrated under reduced pressure. Purification by flash column chromatography (silica, 50:50:2 hexanes/ethyl acetate/acetic acid) afforded 3-iodo-5-(methoxycarbonyl)benzoic acid (4.48 g): 1H NMR (500 MHz, DMSO-d6): δ 13.49 (br s, 1H), 8.45-8.38 (m, 3H), 3.83 (s, 3H); ESI-MS (m/z): 305 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b9e365e738df4d5f94ed7d7af91e7e2d
출처 메모uspto-grants-2010_06