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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 404151생성일: 2026년 10월 24일

Benzyl Bromide → 5-(Benzyloxy)-2-bromopyridine

https://huagongshe.com/ko/reaction/404151

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Ethyl AcetateHCID 8857—
반응물Sodium hydrideHCID 24758—
반응물2-Bromo-5-hydroxypyridineHCID 2762865—
용매DimethylformamideHCID 6228—
생성물5-(Benzyloxy)-2-bromopyridineHCID 1609469672%

반응 단계

2-Bromo-5-hydroxypyridine (347 mg, 2 mmol) in DMF (3 mL) was added dropwise over a period of 10 min to a suspension of NaH (88 mg, 2.3 mmol) in DMF (2 mL) at 0° C. under Ar(g). The reaction mixture was then stirred at rt for 10 min, after which it was again cooled down at 0° C., and benzyl bromide (0.25 mL, 2.1 mmol) was added. The reaction mixture was stirred at rt for 2.5 h, after which it was poured onto brine (20 mL) and EtOAc (20 mL) was added. The phases were separated and the aqueous phase was extracted with EtOAc (20 mL). The organic phases were combined, dried over MgSO4, filtered and subsequently evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography eluting with hexane/EtOAc (95:5 to 90:10) to furnish I as a colourless oil (380 mg, 72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748458B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-a5c72394a02a403c9619268dfe3b6390
출처 메모uspto-grants-2014_06