戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 618作成日:2026年10月23日

Bromobenzene → Diphenylpyrrolidine

https://huagongshe.com/ja/reaction/618

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-PhenylpyrrolidineHCID 261892—
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DiphenylpyrrolidineHCID 1121835290.18%

反応条件

温度100 °C

反応手順

Caesium carbonate (553 mg, 1.70 mmol) was added to bromobenzene (0.059 mL, 0.57 mmol) and 2-phenylpyrrolidine (100 mg, 0.68 mmol) in 1,4-dioxane (2 mL). The reaction was degassed and Tris(dibenzylideneacetone)?dipalladium(0) (12.96 mg, 0.01 mmol) and dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine (RuPhos) (13.21 mg, 0.03 mmol) were added. The resulting solution was stirred at 100 °C for 16 hours. LCMS showed the formation of the product. 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. NMR confirmed the presence of the product. The crude product was purified by flash silica chromatography, elution gradient 0 to 15% DCM in MeOH. Pure fractions were evaporated to dryness to afford 1,2-diphenylpyrrolidine (114 mg, 90 %) as a brown oil.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-9faf2ea031204c63b2d52d8ff6231013
出典メモ750 AstraZeneca ELN dataset