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HRID 2802作成日:2026年10月23日

Methyl iodide → 4-Bromo-1,3,5-trimethylpyrazole

https://huagongshe.com/ja/reaction/2802

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物4-bromo-3,5-dimethyl-1H-pyrazoleHCID 76937—
反応物Sodium BicarbonateHCID 516892—
反応物HCID 178418361HCID 178418361—
溶媒DimethylformamideHCID 6228—
生成物4-Bromo-1,3,5-trimethylpyrazoleHCID 519181—

反応手順

4-Bromo-3,5-dimethylpyrazole (10 g) in dry dimethylformamide (50 ml) was added to a stirred suspension of sodium hydride (1.8 g) in dry dimethylformamide at 0° C. When the evolution of hydrogen was complete, iodomethane (8.9 g) was added dropwise. The mixture was allowed to warm to room temperature and after 30 minutes saturated aqueous sodium hydrogen carbonate (5 ml) was added. Following evaporation under high vacuum, the residue was purified by column chromatography to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731335
出典データセットuspto-grants-1998_03
ORD IDord-ac7f5eb35ef547d1a557dea38319f19e
出典メモuspto-grants-1998_03