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HRID 23318作成日:2026年10月24日

(E)-1,3-Dichloropropene → (E)-2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methyl-6-(3-chloroprop-2-enyloxy)pyridine

https://huagongshe.com/ja/reaction/23318

反応式

関与物質

役割名称HCID仕込み量
反応物(E)-1,3-DichloropropeneHCID 24726—
反応物Sodium hydrideHCID 24758—
反応物HCID 178429419HCID 178429419—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl acetate pentaneHCID 22335286—
生成物(E)-2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methyl-6-(3-chloroprop-2-enyloxy)pyridineHCID 1547717452.3%

反応手順

A mixture of 6-hydroxy-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methylpyridine (0.9 g, 3.3 mmol) and NaH (60% in oil, 0.16 g, 4 mmol) in acetonitrile (20 ml) and DMF (1 ml) is stirred for 10 min at ambient temperature and (E)-1,3-dichloropropene (0.4 g, 3.6 mmol) is added. After stirring for 60 h at ambient temperature, the remaining NaH is deactivated and the resulting mixture is diluted with pentane/ethyl acetate (by volume ration 1/1) and filtered through a bed of silica gel. The filtrate is washed with water. The organic layer is dried with anhydrous magnesium sulfate, filtered and evaporated in vacuo. Purification by flash chromatography (silica gel: pentane/ethyl acetate 9/1 v/v) yields the title compound (0.6 g, 52% yield) as an colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852673B2
出典データセットuspto-grants-2005_02
ORD IDord-1a51b45be5a940eea36ea661e6865feb
出典メモuspto-grants-2005_02