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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23318생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물(E)-1,3-DichloropropeneHCID 24726—
반응물Sodium hydrideHCID 24758—
반응물HCID 178429419HCID 178429419—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
용매Ethyl acetate pentaneHCID 22335286—
생성물(E)-2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methyl-6-(3-chloroprop-2-enyloxy)pyridineHCID 1547717452.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852673B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-1a51b45be5a940eea36ea661e6865feb
출처 메모uspto-grants-2005_02