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HRID 443435作成日:2026年10月25日

Benzyl Chloride → 5-(Benzyloxy)-2-methylpyridine

https://huagongshe.com/reaction/443435

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物2-Methyl-5-hydroxypyridineHCID 14275—
反応物Sodium hydrideHCID 24758—
溶媒DimethylformamideHCID 6228—
生成物5-(Benzyloxy)-2-methylpyridineHCID 12397251—

反応手順

The solution of 32.7 g of 2-methyl-5-hydroxy-pyridine in 300 ml of dimethylformamide is added to a suspension of 12.8 g of sodium hydride (57% mineral oil dispersion) in 150 ml of dimethylformamide, with stirring. Then the mixture is heated to 100° and maintained at 100° for 18 hours. After that, the mixture is cooled to room temperature and to the cooled mixture is added a solution of 49.8 g of benzyl chloride in 100 ml of dimethylformamide over a period of 30 minutes. The mixture is then refluxed for 7 hours, cooled and then evaporated to a residue. The residue is partitioned between water and ether, the layers are separated and the water layer extracted with ether. The ether layer is combined with ether extract, dried over sodium sulfate, filtered and the ethereal filtrate is distilled off. The residue is distilled to yield 5-benzyloxy-2-methyl-pyridine, boiling at 100°-102°/0.02 mm/Hg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04260620
出典データセットuspto-grants-1981_04
ORD IDord-477c2ffbdc5844ecb6688385d1666f9c
出典メモuspto-grants-1981_04