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HRID 917674作成日:2026年10月27日

Dimethyl Sulfoxide → 2-Acetyl-6-methylpyridine

https://huagongshe.com/reaction/917674

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物1-(6-Methylpyridin-2-yl)ethanolHCID 353138—
溶媒DichloromethaneHCID 6344—
生成物2-Acetyl-6-methylpyridineHCID 13887292%

反応条件

温度-75 °C

反応手順

To a −75° C. solution of oxalyl chloride (20 mL, 225 mmol, 1.1 equiv) in methylene chloride (300 mL) was slowly added a solution of dimethylsulfoxide (32 mL, 2.2 equiv) in methylene chloride (400 mL) over 1 hour. The resulting solution was stirred at −75° C. for 10 min,and then slowly treated with a solution of 1-(6-methyl-pyridin-2-yl)-ethanol (28 g, 204 mmol, 1 equiv) in methylene chloride (600 mL). The reaction mixture was stirred for 10 min at the same temperature, and then slowly treated with triethylamine (140 mL, 1.02 mol, 5 equiv). The resulting mixture was warmed to 20° over 2 hours, and then quenched with water (500 mL). The organic phase was separated, dried over magnesium sulfate and concentrated in vacuo to yield the crude material. Silica gel chromatography (3:1 hexanes/ethyl acetate) yielded 1-(6-Methyl-pyridin-2-yl)-ethanone (25.36 g, 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07273936B2
出典データセットuspto-grants-2007_09
ORD IDord-5928362ea2f2426dbbf9f14fcd235798
出典メモuspto-grants-2007_09