돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244583생성일: 2026년 10월 26일

Benzyl Alcohol → 3-(Benzyloxy)-5-bromopyridine

https://huagongshe.com/reaction/244583

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물3-Bromo-5-hydroxypyridineHCID 599529—
용매TetrahydrofuranHCID 8028—
생성물3-(Benzyloxy)-5-bromopyridineHCID 1538919831.9%

반응 단계

To a vial is added 3-bromo-5-hydroxypyridine (200 mg, 1.15 mmol), benzyl alcohol (137 mg, 1.27 mmol) and triphenylphosphine (332 mg, 1.27 mmol) in THF (5 ml) at 0° C., followed by the addition of diisopropyl azodicarboxylate (256 mg, 1.27 mmol). The reaction mixture is stirred at room temperature for 18 hours. The reaction mixture is concentrated in vacuo. The residue is diluted with EtOAc, washed with sat NaHCO3, water, brine, dried under anhy. Na2SO4, filtered and concentrated. The residue is purified by flash chromatography (SiO2, 0-5% MeOH/CH2Cl2) to afford title compound (97 mg); m/z 264.0, 266.0 [M, M+2H]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658661B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-dee370fb0bb64f7abb21b48bbf5c10cd
출처 메모uspto-grants-2014_02