戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 520841作成日:2026年10月26日

2-Pyridinecarboxaldehyde → (1-Methyl-1H-imidazol-5-yl)(pyridin-2-yl)methanol

https://huagongshe.com/reaction/520841

反応式

関与物質

役割名称HCID仕込み量
反応物2-PyridinecarboxaldehydeHCID 14273—
反応物5-Bromo-1-methyl-1H-imidazoleHCID 1515258—
反応物HCID 178461733HCID 178461733—
溶媒TetrahydrofuranHCID 8028—
生成物(1-Methyl-1H-imidazol-5-yl)(pyridin-2-yl)methanolHCID 86715604—

反応条件

温度0 °C

反応手順

A solution of isopropylmagnesium chloride/lithium chloride complex (1.3 M in THF, 19.5 mL, 25.35 mmol) was added dropwise by syringe to a solution of 5-bromo-1-methyl-1H-imidazole (4.12 g, 25.58 mmol) in dry THF (130 mL) at 0° C. After 15 minutes, the Grignard solution was added via cannulation to a solution of picolinaldehyde (2.0 ml, 20.93 mmol) in dry THF (55 mL) at 0° C. The reaction mixture was stirred for 5 minutes at 0° C., then warmed to room temperature for 1 hour. The reaction mixture was then cooled in an ice bath and quenched with saturated aqueous ammonium chloride. The mixture was partitioned between brine and ethyl acetate. The separated aqueous phase was further extracted with ethyl acetate. The organic phase was dried (Na2SO4), filtered, and concentrated. The crude product was purified by flash column chromatography (silica gel, 0-5% MeOH-DCM) to provide the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328095B2
出典データセットuspto-grants-2016_05
ORD IDord-ce3ec1c8d3974353a11504b793e9359d
出典メモuspto-grants-2016_05