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HRID 569作成日:2026年10月23日

Bromobenzene → 1,2-Diphenylpiperidine

https://huagongshe.com/ja/reaction/569

反応式

関与物質

役割名称HCID仕込み量
反応物BromobenzeneHCID 7961—
反応物2-PhenylpiperidineHCID 103020—
試薬Cesium carbonateHCID 10796—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
触媒2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
溶媒1,4-DioxaneHCID 31275—
生成物1,2-DiphenylpiperidineHCID 1243476415.56%

反応条件

温度100 °C

反応手順

Caesium carbonate (556 mg, 1.71 mmol) was added to bromobenzene (0.060 mL, 0.57 mmol) and 2-phenylpiperidine (110 mg, 0.68 mmol) in 1,4-dioxane (2 mL). The reaction was degassed and Tris(dibenzylideneacetone)?dipalladium(0) (13.01 mg, 0.01 mmol) and dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine (RuPhos) (13.26 mg, 0.03 mmol) were added. The resulting solution was stirred at 100 °C for 16 hours. LCMS showed The reaction mixture was diluted with EtOAc, and washed with water. The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 15% MeOH in DCM. Pure fractions were evaporated to dryness to afford 1,2-diphenylpiperidine (21.00 mg, 15.56 %) as a yellow oil. f0 = 19 mg bromobenzene f1 = 21 mg product The reaction was abandonned.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-bd4700a79525457dbcfd3c5e1368118f
出典メモ750 AstraZeneca ELN dataset