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HRID 52182作成日:2026年10月23日

3-Pyridinecarboxaldehyde → Pyridin-3-yl(thiophen-2-yl)methanol

https://huagongshe.com/ja/reaction/52182

反応式

関与物質

役割名称HCID仕込み量
反応物3-PyridinecarboxaldehydeHCID 10371—
反応物Chloroform methanolHCID 21584188—
反応物HCID 178418439HCID 178418439—
溶媒TetrahydrofuranHCID 8028—
生成物Pyridin-3-yl(thiophen-2-yl)methanolHCID 65049962.2%

反応条件

温度-78 °C

反応手順

To a solution of 3-pyridinecarboxaldehyde (5.0 mL, 53 mmol) in THF at -78° C. was added 2-thienyllithium (1.0M in THF. 64 mL, 64 mmol) and the reaction mixture was stirred for 2 hours at -78° C. The reaction mixture was quenched with saturated aqueous NH4Cl and extracted with ether. The organic phase was dried over MgSO4, filtered, and concentrated in vacuo. Chromatography on silica gel (5%, then 10% methanol/CHCl3) gave 2-(3-pyridylhydroxymethyl)thiophene (6.30 g, 62% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616596
出典データセットuspto-grants-1997_04
ORD IDord-821002a002e645fc8b3d520076f6a82a
出典メモuspto-grants-1997_04