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HRID 335084作成日:2026年10月26日

Benzoyl Peroxide → 2-(1-Bromoethyl)pyridine

https://huagongshe.com/reaction/335084

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl PeroxideHCID 7187—
反応物2-EthylpyridineHCID 7523—
反応物N-bromobutanimideHCID 67184—
溶媒Carbon TetrachlorideHCID 5943—
生成物2-(1-Bromoethyl)pyridineHCID 1537365749.9%

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883828B2
出典データセットuspto-grants-2014_11
ORD IDord-b6cd741540ee4b83a966361d0022c63f
出典メモuspto-grants-2014_11