돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 440981생성일: 2026년 10월 25일

Water → 5-(2-Trifluoromethylphenyl)-4-pentynenitrile

https://huagongshe.com/reaction/440981

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물Benzene, 1-iodo-2-(trifluoromethyl)-HCID 67957—
반응물4-Cyano-1-butyneHCID 140560—
촉매Copper iodideHCID 83717—
촉매HCID 178418476HCID 178418476—
용매AcetonitrileHCID 6342—
생성물5-(2-Trifluoromethylphenyl)-4-pentynenitrileHCID 1995553892.9%

반응 단계

Under a nitrogen atmosphere, a solution of 15.0 grams (0.055 mole) of 2-trifluoromethylphenyl iodide, 4.8 grams (0.061 mole) of 4-pentynenitrile, 30.6 mL (0.22 mole) of triethylamine, 0.4 gram (0.0006 mole) of bis(triphenylphosphine)palladium(II) chloride, and 0.1 gram (0.0006 mole) of copper(II) iodide in 50 mL of acetonitrile was stirred at ambient temperature for 5 hours. After this time, gas chromatographic analysis (GC) of the reaction mixture indicated that the reaction was about 60% complete. The reaction mixture was warmed to 40°-45° C., where it was stirred for 16 hours. After this time the reaction mixture was poured into 300 mL of water, and the mixture was extracted with two 100 mL portions of diethyl ether. The combined extracts were washed with aqueous dilute hydrochloric acid and then were dried with magnesium sulfate. The mixture was filtered and concentrated under reduced pressure to a residual oil. The oil was subjected to column chromatography on silica gel. Elution was accomplished using 1:1-methylene chloride and petroleum ether. The product-containing fractions were combined and concentrated under reduced pressure, yielding 11.4 grams of 5-(2-trifluoromethylphenyl)-4-pentynenitrile. The NMR spectrum was consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05521192
출처 데이터셋uspto-grants-1996_05
ORD IDord-9a62fb6a39604dc586b353f75b6b63db
출처 메모uspto-grants-1996_05