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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 387835생성일: 2026년 10월 26일

Hydrochloric Acid → 2-Chloro-3-hydroxy-6-iodopyridine

https://huagongshe.com/reaction/387835

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium IodideHCID 5238—
반응물TosylchloramideHCID 31388—
반응물2-Chloro-3-pyridinolHCID 81136—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물2-Chloro-3-hydroxy-6-iodopyridineHCID 1077741791.2%

반응 단계

After dissolving 2-chloro-3-hydroxypyridine (5.00 g, 38.6 mmol) and sodium iodide (5.79 g, 38.6 mmol) in dimethylformamide (70 ml), Chloramine T (10.9 g, 38.6 mmol) was added while cooling on ice, and then the mixture was stirred at room temperature for 1 hour. Upon adding 2N aqueous hydrochloric acid (19.3 ml, 38.6 mmol) after the reaction, the reaction solution was distributed between ethyl acetate and water, the organic layer was washed with water and saturated saline and dried over anhydrous magnesium sulfate, the drying agent was filtered off and the filtrate was distilled off under reduced pressure. The obtained crude product was subjected to silica gel column chromatography (eluent-ethyl acetate:hexane=1:2), and the fraction containing the target substance was concentrated to obtain the title compound (9.00 g, 35.2 mmol, 91%) as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372981B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-8aaf834e55664c51bfd51805daae7681
출처 메모uspto-grants-2013_02