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HRID 349978作成日:2026年10月26日

Thionyl Chloride → 2-[4-(Chloromethyl)-3-methyl-1H-pyrazol-1-YL]pyridine

https://huagongshe.com/reaction/349978

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[3-Methyl-1-(pyridin-2-yl)-1H-pyrazol-4-yl]methanolHCID 23076503—
溶媒TolueneHCID 1140—
生成物2-[4-(Chloromethyl)-3-methyl-1H-pyrazol-1-YL]pyridineHCID 1786128994%

反応条件

温度70 °C

反応手順

A mixture of 3-methyl-1-(2-pyridyl)-1H-pyrazol-4-ylmethanol (3.00 g), thionyl chloride (2.5 ml) and toluene (50 ml) was stirred at 70° C. for 2 hours. The reaction mixture was concentrated under reduced pressure, and saturated aqueous sodium bicarbonate solution was added to the residue, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4) and concentrated to obtain 4-chloromethyl-3-methyl-1-(2-pyridyl)-1H-pyrazole (3.10 g, yield 94%) as a colorless oily substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07179823B1
出典データセットuspto-grants-2007_02
ORD IDord-6682ecdb3dad40cb984336166effd6f8
出典メモuspto-grants-2007_02