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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → Ethyl 5-bromo-1H-indole-7-carboxylate

HRID 656003
ノート
印刷プレビュー

反応式

HRID 656003 の反応式
C(C1C(=O)C(Cl)=C(Cl)C(=O)C=1C#N)#N.[Br:15][C:16]1[CH:17]=[C:18]2[C:22](=[C:23]([C:25]([O:27][CH2:28][CH3:29])=[O:26])[CH:24]=1)[NH:21][CH2:20][CH2:19]2>C(Cl)(Cl)Cl>[Br:15][C:16]1[CH:17]=[C:18]2[C:22](=[C:23]([C:25]([O:27][CH2:28][CH3:29])=[O:26])[CH:24]=1)[NH:21][CH:20]=[CH:19]2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 59332604Ethyl 5-bromoindoline-7-carboxylate

生成物 1

HCID 59332585Ethyl 5-bromo-1H-indole-7-carboxylate収率 68,380.797%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

DDQ (119.3 g. 525.7 mmol) was added in several portions to a solution of ethyl 5-bromo-2,3-dihydro-1H-indole-7-carboxylate (129.1 g, 0.48 mmol) in CHCl3 (1500 mL) and the mixture was stirred for 2 h. The reaction was filtered and the solid was washed with CHCl3 (3×500 mL). The filtrate was washed with 5% NaOH (3×500 mL), H2O (500 mL) and brine (500 mL) then dried over Na2SO4. The solution was evaporated and the residue was recrystallized with EtOH, giving 88 g (69%) of the title compound.

後処理

  1. filtrationThe reaction was filtered
  2. washthe solid was washed with CHCl3 (3×500 mL)
  3. washThe filtrate was washed with 5% NaOH (3×500 mL), H2O (500 mL) and brine (500 mL)
  4. dry with materialthen dried over Na2SO4
  5. customThe solution was evaporated
  6. customthe residue was recrystallized with EtOH

出典と根拠

ORDレコード
ord-8c507906e8db429abed27d614af095c7
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08071584B2

反応ノート

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