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HRID 77901作成日:2026年10月23日

Dimethylformamide → 2-(4-Bromo-benzyloxy)-5-methyl-pyridine

https://huagongshe.com/ja/reaction/77901

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-5-methylpyridineHCID 2774635—
溶媒WaterHCID 962—
生成物2-(4-Bromo-benzyloxy)-5-methyl-pyridineHCID 5925544959.3%

反応手順

To an N,N-dimethylformamide (50.0 mL) solution of 4-bromobenzyl alcohol (4.54 g, 24.3 mmol) was added sodium hydride (1.00 g, 25.0 mmol, 60% in oil) under nitrogen atmosphere at 0° C., which was stirred for 30 minutes at room temperature. 2-Fluoro-5-methylpyridine (1.80 g, 16.2 mmol) was then added at 0° C., and stirred for 5 hours 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 and washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:15) to obtain the title compound (2.67 g, 59.3%).

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-facb86b0ae294aae8f86b7ad66b231a8
出典メモuspto-grants-2014_09