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HRID 77896作成日:2026年10月23日

Dimethylformamide → 2-(4-Bromo-benzyloxy)4-methyl-pyridine

https://huagongshe.com/ja/reaction/77896

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物4-Bromobenzyl alcoholHCID 70119—
反応物2-Fluoro-4-methylpyridineHCID 2737403—
溶媒WaterHCID 962—
生成物2-(4-Bromo-benzyloxy)4-methyl-pyridineHCID 5925528858.8%

反応手順

To a mixture of 4-bromobenzyl alcohol (4.54 g, 24.3 mmol) and N,N-dimethylformamide (50.0 mL) were added sodium hydride (1.00 g, 25.0 mmol, 60% in oil) was added at 0° C. under nitrogen atmosphere, which was stirred for 50 minutes at room temperature. 2-Fluoro-4-methylpyridine (1.80 g, 16.2 mmol) was then added thereto at 0° C., and stirred for 2 hours and 30 minutes at room temperature. Water was added to the reaction solution at room temperature, which was then extracted with ethyl acetate. The organic layer was separated, washed with saturated aqueous sodium chloride, and filtered. The filtrate was evaporated under a reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:15) to obtain the title compound (2.65 g, 58.8%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841327B2
出典データセットuspto-grants-2014_09
ORD IDord-79efb6ff36ff47b189d35a939edd6e29
出典メモuspto-grants-2014_09