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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Bromobenzene → Diphenylpyrrolidine

HRID 618
ノート
印刷プレビュー

反応式

HRID 618 の反応式
Brc1ccccc1.c1ccc(C2CCCN2)cc1>C1COCCO1.CC(C)Oc1cccc(OC(C)C)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C([O-])[O-].[Cs+].[Cs+].[Pd].[Pd]>c1ccc(C2CCCN2c2ccccc2)cc1
参加物反応条件実験手順出典と根拠反応ノート

参加物

7

反応物 2

HCID 7961BromobenzeneHCID 2618922-Phenylpyrrolidine

生成物 1

HCID 11218352Diphenylpyrrolidine収率 90.18%

試薬・触媒・溶媒 4

HCID 10796Cesium carbonate試薬HCID 9811564Bis(dibenzylideneacetone)palladium触媒
HCID 16217985
2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl
触媒
HCID 312751,4-Dioxane溶媒

反応条件

温度
100 °C

実験手順

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.

出典と根拠

ORDレコード
ord-9faf2ea031204c63b2d52d8ff6231013
出典データセット
750 AstraZeneca ELN dataset
元リンク
出典を表示

反応ノート

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