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HRID 128602作成日:2026年10月25日

Ethyl Bromide → 3-Ethoxy-2-methylpyridine

https://huagongshe.com/reaction/128602

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl BromideHCID 6332—
反応物2-Methylpyridin-3-olHCID 70719—
反応物SodiumHCID 5360545—
溶媒EthanolHCID 702—
生成物3-Ethoxy-2-methylpyridineHCID 12875015—

反応手順

Sodium metal (46.2 g) was dissolved in absolute ethanol (1 l) with stirring under nitrogen. 3-Hydroxy-2-methylpyridine (200 g prepared as described in C.A. 48, P4597 h) was added. The mixture was stirred at ambient temperature for 30 minutes and then a solution of bromoethane (350 ml) in absolute ethanol (100 ml) was added. The mixture was boiled under reflux for 5 hours then cooled and filtered. The filtrate was evaporated and the residue partitioned between dichloromethane and water. The organic layer was separated off and the aqueous layer extracted with dichloromethane. The combined organic extracts were dried and evaporated. The residue was distilled to give 3-ethoxy-2-methylpyridine b.p. 80°-84° C. (20 mmHg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464781
出典データセットuspto-grants-1995_11
ORD IDord-c33f66750f284082bf393a82d40ba091
出典メモuspto-grants-1995_11