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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335084생성일: 2026년 10월 25일

Benzoyl Peroxide → 2-(1-Bromoethyl)pyridine

https://huagongshe.com/reaction/335084

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물2-EthylpyridineHCID 7523—
반응물N-bromobutanimideHCID 67184—
용매Carbon TetrachlorideHCID 5943—
생성물2-(1-Bromoethyl)pyridineHCID 1537365749.9%

반응 단계

2-Ethylpyridine (20.0 g, 186.65 mmol) was placed in carbon tetrachloride (830 mL) and benzoyl peroxide (4.5211 g, 18.665 mmol) and 1-bromopyrrolidine-2,5-dione (33.221 g, 186.65 mmol) were added. The reaction mixture was heated to reflux for 18 hours, then cooled to room temperature and filtered. The filtrate was concentrated and the residue was purified over a plug of silica to give 2-(1-bromoethyl)pyridine (17.312 g, 49.9%). 1H NMR (CDCl3) δ 8.58 (d, 1H), 7.69 (td, 1H), 7.76 (d, 1H), 7.20 (dd, 1H), 5.24 (q, 1H), 2.08 (d, 3H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883828B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-b6cd741540ee4b83a966361d0022c63f
출처 메모uspto-grants-2014_11