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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 → 1,2-Diphenylpiperidine

HRID 569
ノート
印刷プレビュー

反応式

HRID 569 の反応式
Brc1ccccc1.c1ccc(C2CCCCN2)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(C2CCCCN2c2ccccc2)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 1030202-Phenylpiperidine

生成物 1

HCID 124347641,2-Diphenylpiperidine収率 15.56%

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 (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.

出典と根拠

ORDレコード
ord-bd4700a79525457dbcfd3c5e1368118f
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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