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HRID 383839作成日:2026年10月25日

4-Toluenesulfonyl chloride → 2-(6-Methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/383839

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物TriethylamineHCID 8471—
反応物2-(6-Methoxypyridin-2-yl)ethan-1-olHCID 15319871—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物2-(6-Methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonateHCID 59636776—

反応手順

A solution of 2-(6-methoxypyridin-2-yl)ethanol (0.23 g, 1.50 mmol), 4-dimethylaminopyridine (0.028 g, 0.23 mmol), triethylamine (0.63 mL, 4.50 mmol) and p-toluenesulfonyl chloride (0.34 g, 1.80 mmol) in dry dichloromethane (5 mL) was stirret at rt over night. The solvent was removed in vacuo. Ethyl acetate and water were added. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried (Na2SO4) and concentrated. The product was purified by flash chromatography (SiO2; heptane/EtOAc, gradient 0-100%). Yield: 0.18 g (38%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367676B2
出典データセットuspto-grants-2013_02
ORD IDord-6545365a0b0348e9849fae3bfbf04624
出典メモuspto-grants-2013_02