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HRID 71724作成日:2026年10月26日

Benzyl Bromide → 2-(Benzyloxy)-4-bromopyridine

https://huagongshe.com/reaction/71724

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物4-Bromo-2-hydroxypyridineHCID 817115—
触媒HCID 178418647HCID 178418647—
溶媒BenzeneHCID 241—
生成物2-(Benzyloxy)-4-bromopyridineHCID 53217389—

反応条件

温度50 °C

反応手順

A mixture of 4-Bromo-1H-pyridin-2-one (0.613 g), silver carbonate (0.63 g) and benzyl bromide (0.50 mL) in benzene (10 mL) was heated at 50° C. for 24 hours, protected from light. Reaction mixture stirred ambient temperature for 16 hours. Reaction mixture was filtered through a pad of CELITE, which was washed ethyl acetate. The filtrate was concentrated and purified by flash column chromatography (silica gel, 0 to 10% ethyl acetate/hexanes) to give 2-Benzyloxy-4-bromo-pyridine (0.6043 g): LCMS-ESI+: calc'd for C12H11BrNO: 265.12 (M+H+). Found: 263.8, 265.8 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822430B2
出典データセットuspto-grants-2014_09
ORD IDord-b18655ce0d4f456aa6bcc15e60d2d09f
出典メモuspto-grants-2014_09