戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 83113作成日:2026年10月23日

Sodium Chloride → 2-Methyl-6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridine

https://huagongshe.com/ja/reaction/83113

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Sodium hydrideHCID 24758—
反応物2-Fluoro-6-methylpyridineHCID 96090—
反応物(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methyl-6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridineHCID 5751983148.2%

反応手順

To a suspension of sodium hydride (55% dispersion in mineral oil, 48 mg, 1.1 mmol) in THF (1.5 mL) was added a solution of (5-methyl-3-phenyl-isoxazol-4-yl)-methanol (189 mg, 1.0 mmol) in THF (3 mL) at 0° C. and the reaction mixture warmed to room temperature over 30 min. Then a solution of 2-fluoro-6-methylpyridine (122 mg, 1.1 mmol) in THF (3 mL) was added dropwise at 0° C. and the reaction mixture was stirred at room temperature overnight. The reaction mixture was then poured into aqueous sodium chloride (saturated) and the mixture was extracted with ethyl acetate. The combined organic layers were then washed with water and brine and then dried over sodium sulfate, filtered and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 4:1) afforded the title compound (135 mg, 48%) which was obtained as a yellow oil. MS: m/e=281.1 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846719B2
出典データセットuspto-grants-2014_09
ORD IDord-97dc3e647fb34eddb9b3a2979bd6cb4a
出典メモuspto-grants-2014_09