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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1057261생성일: 2026년 10월 26일

Toluene → 4-[(4-Pentylphenyl)ethynyl]phenol

https://huagongshe.com/reaction/1057261

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물4-IodophenylacetateHCID 141793—
반응물1-Ethynyl-4-pentylbenzeneHCID 2775131—
촉매Copper iodideHCID 83717—
촉매HCID 178418476HCID 178418476—
용매DiisopropylamineHCID 7912—
생성물4-[(4-Pentylphenyl)ethynyl]phenolHCID 18671138—

반응 단계

4-Pentylphenylacetylene (10.5 g, 61.4 mmol), 4-acetoxyphenyl iodide (16.1 g, 61.4 mmol), a catalytic amount of Pd(PPh3)2Cl2 and a catalytic amount of copper iodide were stirred in diisopropylamine (100 ml) at 70° C. After 5 minutes, a precipitate was seen and the mixture became unstirrable, toluene (100 ml) was added. The mixture was stirred at room temperature for 24 hours and then evaporated to dryness on a rotary evaporator. The residue was redissolved in aqueous potassium hydroxide ethanolic solution and stirred at 70° C. overnight. The mixture was evaporated to dryness, then partitioned between ethyl acetate and water, the organic phase was removed, dried and evaporated. The residue was purified by flash column chromatography using DCM as eluant. A pink coloured solid was left after evaporation of the appropriate fractions. Yield=10.4 g, 64%. 1H-NMR and IR spectroscopy gave the expected signals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06514578B1
출처 데이터셋uspto-grants-2003_02
ORD IDord-fbc96aea378f44dca8347db3b9ca696d
출처 메모uspto-grants-2003_02