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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15037생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 2-Bromo-5-(2-tetrahydropyranyloxy)pyridine

https://huagongshe.com/ko/reaction/15037

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물2-Bromo-5-hydroxypyridineHCID 2762865—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물2-Bromo-5-(2-tetrahydropyranyloxy)pyridineHCID 8661489155%

반응 단계

A mixture of 2-bromo-5-hydroxypyridine (1.0 g, 5.75 mmols), 3,4-dihydro-2H-pyran (0.80 mL, 8.77 mmols) and p-toluenesulfonic acid (110 mg, 0.578 mmol) was stirred overnight in dichloromethane (20 mL) at room temperature. The reaction liquid was diluted with chloroform, washed with saturated brine and dried over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the resulting residue was purified on silica gel column chromatography (C-300; ethyl acetate:hexane=1:20-1:10) to provide the title compound (0.81 g, 55%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732456B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-22d50e01a3bc4b4d88cece5f10779ccd
출처 메모uspto-grants-2010_06