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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 712472생성일: 2026년 10월 24일

Benzyl Bromide → (3-(Benzyloxy)pyridin-2-yl)methanol

https://huagongshe.com/ko/reaction/712472

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium HydroxideHCID 14797—
반응물3-Hydroxypyridine-2-methanolHCID 84169—
용매EthanolHCID 702—
생성물(3-(Benzyloxy)pyridin-2-yl)methanolHCID 1321754065%

반응 단계

To a solution of 3-hydroxy-2-(hydroxymethyl)pyridine (10.00 g) and KOH (7.00 g) in anhydrous EtOH was added benzyl bromide (7.30 mL) at room temperature under stirring. The reaction mixture was heated to reflux for 24 h, then cooled to rt and filtered. The filtrate was concentrated in vacuo and the residue was chromatographed with a silica gel column (eluting agent: 20:1 (v/v) DCM/MeOH) to give the title compound as a pale yellow solid (7.50 g, 65.00%), HPLC: 95.00%. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 216.4 (M+1); 1H NMR (400 MHz, CDCl3) δ: 4.39 (br s, 1H), 4.82 (s, 2H), 5.11 (s, 2H), 7.16-7.17 (m, 2H), 7.34-7.40 (m, 5H), 8.15-8.17 (m, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181277B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-7452e675d20641e6b0762bc342aefbf1
출처 메모uspto-grants-2015_11