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HRID 85186作成日:2026年10月24日

Dimethylformamide → 6-Methyl-3-pyridinecarboxaldehyde

https://huagongshe.com/ja/reaction/85186

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物5-Bromo-2-methylpyridineHCID 1201020—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物6-Methyl-3-pyridinecarboxaldehydeHCID 1019256672%

反応手順

To a solution of 5-bromo-2-methylpyridine (151; 10 g, 58.1 mmol) in THF (150 mL) was added n-BuLi (2.5 M, 25.6 mL) at −78° C. The reaction mixture was stirred at this temperature for 1 h. DMF (1.30 mL) was then added and the resulting reaction mixture was stirred for 1 h at −78° C. The reaction was quenched by the addition of aq. NH4Cl. Upon warming to room temperature, the mixture was extracted with EtOAc. The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. The resulting residue was purified by chromatography to afford 6-methylnicotinaldehyde 152 (5.0 g, 72%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846947B2
出典データセットuspto-grants-2014_09
ORD IDord-2b79cc6d18e6464aaf106b76420e7363
出典メモuspto-grants-2014_09