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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1181생성일: 2026년 10월 26일

Water → 4'-(trans-4-Propylcyclohexyl)-3,4-difluorobiphenyl

https://huagongshe.com/reaction/1181

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-Bromo-1,2-difluorobenzeneHCID 67675—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물4-(4-Propylcyclohexyl)-phenyltrimethoxysilaneHCID 10860253—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물4'-(trans-4-Propylcyclohexyl)-3,4-difluorobiphenylHCID 61230694.5%

반응 단계

To 0.645 g (2 mmol) of 4-(4-propylcyclohexyl)-phenyltrimethoxysilane (Ih) was added 2.1 ml of TBAF (2.1 mmol, 1M in THF) under nitrogen, and the mixture was stirred at room temperature for 30 minutes. After the solvent was removed under reduced pressure, a solution of 3,4-difluorobromobenzene (0.463 g, 2.4 mmol) in toluene (1 ml) was added, followed by the addition of a suspension of tetrakis(triphenylphosphine)palladium(0) (0.116 g, 0.1 mmol) in toluene (3 ml). The resulting mixture was refluxed for 3 hours. After cooling, to the reaction mixture were added water and toluene. The organic layer was separated and the aqueous layer was extracted with toluene three times. The combined organic layer was dried over magnesium sulfate. After the magnesium sulfate was removed by filtration, the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (heptane) to obtain 0.594 g (40%) of white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723621
출처 데이터셋uspto-grants-1998_03
ORD IDord-f5c19c1716b641f7a3721e4238a2fc65
출처 메모uspto-grants-1998_03