돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15058생성일: 2026년 10월 26일

Triethylamine → 2-Chloro-4-[(4-fluorophenoxy)methyl]pyridine

https://huagongshe.com/reaction/15058

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-FluorophenolHCID 9732—
반응물Potassium CarbonateHCID 11430—
반응물Methanesulfonyl chlorideHCID 31297—
반응물(2-Chloropyridin-4-yl)methanolHCID 7062237—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-Chloro-4-[(4-fluorophenoxy)methyl]pyridineHCID 6229979951%

반응 단계

Triethylamine (1.2 mL, 8.4 mmols) was added to a mixture of (2-chloro-4-pyridinyl)methanol (1.0 g, 7.0 mmols), methanesulfonyl chloride (0.6 mL, 7.7 mmols) and ethyl acetate (20 mL) under cooling with ice, and stirred at room temperature for 2 hours. Filtering the reaction liquid, the filtrate was concentrated. To the resulting residue, 4-fluorophenol (0.94 g, 8.4 mmols), potassium carbonate (1.93 g, 14.0 mmols) and N,N-dimethylformamide (20 mL) were added and s at 80° C. for 20 hours. Cooling the reaction liquid to room temperature, ethyl acetate was added thereto, followed by washing with saturated aqueous sodium hydrogencarbonate solution and saturated brine and drying over anhydrous sodium sulfate. Concentrating the solvent under reduced pressure, the residue was purified on silica gel column chromatography (KP-Sil, FLASH 40+M, chloroform) to provide the title compound (845 mg, 51%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732456B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3208cf4fa1154931887786da26bad179
출처 메모uspto-grants-2010_06