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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23316생성일: 2026년 10월 23일

Triphenylphosphine → (E)-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methyl-6-(4,4,4-trifluorobut-2-enyloxy)pyridine

https://huagongshe.com/ko/reaction/23316

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물4,4,4-Trifluoro-2-buten-1-olHCID 2777076—
반응물HCID 178429419HCID 178429419—
용매1,4-DioxaneHCID 31275—
용매Ethyl acetate pentaneHCID 22335286—
생성물(E)-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methyl-6-(4,4,4-trifluorobut-2-enyloxy)pyridineHCID 1547717399.4%

반응 단계

A mixture of 6-hydroxy-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methylpyridine (0.8 g, 2.93 mmol), 4,4,4-trifluorobut-2-en-1-ol (0.44 g, 3.5 mmol), triphenylphosphine (0.92 g, 3.51 mmol) and diethyl azodicarboxylate (0.61 g, 3.51 mmol) in dry dioxane (3 ml) is stirred for 1.5 h at ambient temperature. The reaction 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: pentanelethyl acetate 9/1 v/v) yields the title compound (1.11 g, 70% yield) as an colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852673B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-60a2222fb0ff4fdeadd380505f4e7580
출처 메모uspto-grants-2005_02