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HRID 77962作成日:2026年10月25日

Thionyl Chloride → 5-Chloro-2-(chloromethyl)pyridine

https://huagongshe.com/reaction/77962

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物Sodium BicarbonateHCID 516892—
反応物(5-Chloropyridin-2-yl)methanolHCID 20537893—
溶媒DichloromethaneHCID 6344—
生成物5-Chloro-2-(chloromethyl)pyridineHCID 1451715178%

反応手順

To a mixture of (5-chloro-pyridine-2-yl)-methanol (706 mg, 4.92 mmol) described in Manufacturing Example 63-1-1 and dichloromethane (70 mL) was added thionyl chloride (539 μL, 7.38 mmol), which was stirred for 1 hour at room temperature. Saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, which was then extracted with dichloromethane. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (620.0 mg, 78%).

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-d545fe424bee442cbd171484813d9857
出典メモuspto-grants-2014_09