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HRID 1181作成日:2026年10月27日

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

https://huagongshe.com/reaction/1181

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-Bromo-1,2-difluorobenzeneHCID 67675—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物4-(4-Propylcyclohexyl)-phenyltrimethoxysilaneHCID 10860253—
触媒HCID 178418397HCID 178418397—
溶媒TolueneHCID 1140—
生成物4'-(trans-4-Propylcyclohexyl)-3,4-difluorobiphenylHCID 61230694.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723621
出典データセットuspto-grants-1998_03
ORD IDord-f5c19c1716b641f7a3721e4238a2fc65
出典メモuspto-grants-1998_03