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3-Iodobenzyloxybenzene → 2-Methyl-1-(3-phenylmethoxyphenyl)-6-(trifluoromethoxy)indole

HRID 446
ノート
印刷プレビュー

反応式

HRID 446 の反応式
Cc1cc2ccc(OC(F)(F)F)cc2[nH]1.Ic1cccc(OCc2ccccc2)c1>CC(C)(C)P(c1ccccc1-c1ccccc1)C(C)(C)C.CC(C)(C)[O-].Cc1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.[Na+].[Pd].[Pd]>Cc1cc2ccc(OC(F)(F)F)cc2n1-c1cccc(OCc2ccccc2)c1
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 42280193-IodobenzyloxybenzeneHCID 121806692-Methyl-6-(trifluoromethoxy)-1H-indole

生成物 1

HCID 592167202-Methyl-1-(3-phenylmethoxyphenyl)-6-(trifluoromethoxy)indole収率 10.45%

試薬・触媒・溶媒 4

HCID 23676156Sodium t-butoxide試薬HCID 27342152-(Di-tert-butylphosphino)biphenyl触媒
HCID 9811564
Bis(dibenzylideneacetone)palladium
触媒
HCID 1140Toluene溶媒

反応条件

温度
120 °C

実験手順

EN04773-52, _Buchwald coupling, toluene and iodide_ The indole from 4773-25, 1-(benzyloxy)-3-iodobenzene,Pd2(dba)3, JohnPhos and KOtBu were dissolved in toluene. The mixture was warmed at 120 °C for 1h and 50% conversion was observed on NMR*(see attached NMR). The mixture was warmed further 15h at 120°C, still starting material left but the reaction mixture was directly applied to a silica column (heptane 3:1). Product was collected in fraction 22-23 (see attached NMR). Only 19.3 mg (10.45% yield) could be collected but NMR showed correct product. Test reaction with bromide was performed in 4773-53. ######################### *Small amount from reaction mixture was dissolved in CDCl3 and 1HNMR analysis was performed)

出典と根拠

ORDレコード
ord-055c0d9926684c29963cad751105f26e
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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