돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1621439생성일: 2026년 10월 25일

4-Methoxybenzyl alcohol → 3-Bromo-2-fluoro-5-((4-methoxybenzyloxy)methyl)pyridine

https://huagongshe.com/reaction/1621439

반응식

참여 물질

역할이름HCID투입량
반응물4-Methoxybenzyl alcoholHCID 7738—
반응물AluminumHCID 5359268—
반응물3-Bromo-5-(bromomethyl)-2-fluoropyridineHCID 59548244—
촉매Tetrabutylammonium IodideHCID 67553—
촉매HCID 178418778HCID 178418778—
용매AcetonitrileHCID 6342—
생성물3-Bromo-2-fluoro-5-((4-methoxybenzyloxy)methyl)pyridineHCID 5954829124%

반응 단계

3-Bromo-5-(bromomethyl)-2-fluoropyridine (5.63 g, 20.9 mmol) was dissolved in MeCN (135 mL) and 4-methoxybenzyl alcohol (5.20 mL, 41.9 mmol), silver (I) oxide (7.169 g, 30.9 mmol), and tetrabutylammonium iodide (2.208 g, 5.98 mmol) were added. The reaction flask was covered with aluminum foil and the reaction was stirred under nitrogen at room temperature overnight. The reaction was filtered through a pad of Celite® (diatomaceous earth), washing with DCM, MeOH and MeCN. The filtrate was concentrated and purified on a silica gel column (3:1 to 2:1 to 3:2 hexanes/DCM to 3:2 DCM/hexanes to 2:1 DCM/hexanes to 3:1 DCM/hexanes to DCM) to give 3-Bromo-2-fluoro-5-((4-methoxybenzyloxy)methyl)pyridine (1.62 g, 24%). MS (ESI pos. ion) m/z 326/328 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08772480B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-ab5a002a5d574e6f8c2231af6515db9c
출처 메모uspto-grants-2014_07