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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70497생성일: 2026년 10월 25일

Ammonium Chloride → (5-Chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol

https://huagongshe.com/reaction/70497

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물4-BromothioanisoleHCID 66037—
반응물5-Chloro-6-methoxypicolinaldehydeHCID 58452846—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(5-Chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanolHCID 6739610872.3%

반응 단계

n-Butyllithium (2.64 M, 2.9 mL) was added to a solution of 4-bromothioanisole (1.61 g) in tetrahydrofuran (20 mL) at −78° C. in a nitrogen atmosphere, and the mixture was stirred at the same temperature for 30 minutes. A solution of 5-chloro-6-methoxypyridine-2-carbaldehyde (1.14 g) in tetrahydrofuran (10 mL) was added to the reaction solution, followed by stirring for one hour. The reaction solution was poured into a saturated ammonium chloride solution, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered, after which the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1→4:1) to give (5-chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol as a pale yellow oil (1.42 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822503B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f806ee9f51c84a7e8397092246675d0c
출처 메모uspto-grants-2014_09