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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2053729생성일: 2026년 10월 25일

Iodine → Methyl 5-chloro-4-iodo-2-methoxybenzoate

https://huagongshe.com/reaction/2053729

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Sulfuric AcidHCID 1118—
반응물Potassium IodideHCID 4875—
반응물Methyl 4-amino-5-chloro-2-methoxybenzoateHCID 700493—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물Methyl 5-chloro-4-iodo-2-methoxybenzoateHCID 6931479584.2%

반응 조건

온도-1 °C

반응 단계

4-Amino-5-chloro-2-methoxy benzoic acid methyl ester of Step A (5.00 g, 23.2 mmol) was suspended in water (52 mL) and concentrated sulfuric acid (13 mL) was added. The resulting suspension was cooled to −1° C. and a solution of sodium nitrite (1.76 g, 25.5 mmol) in water (10 mL) was added at a rate which maintained the temperature below 0° C., resulting in the formation of a clear yellow solution. A mixture of potassium iodide (4.23 g, 25.5 mmol) and iodine (3.24 g, 12.8 mmol) in water (50 mL) was then added dropwise and the reaction stirred at 0° C. for 1.5 hours. The reaction mixture was warmed to room temperature and extracted with ethyl acetate (200 mL). The combined extracts were washed sequentially with 1 M aqueous sodium thiosulfate, 1 N sodium hydroxide and brine, and dried over anhydrous magnesium sulfate, filtered and concentrated, whereupon the product crystallized out. The resulting orange crystals were suspended in petroleum ether, filtered and dried in vacuo to provide the title compound (6.38 g), m.p. 72-73° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07326700B2
출처 데이터셋uspto-grants-2008_02
ORD IDord-3a411f5e803e4aa8a207f36c820be219
출처 메모uspto-grants-2008_02