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Sodium Iodide → 3-Iodo-5-(4-trifluoromethylphenyl)indole-2-carboxylic acid ethyl ester

HRID 420971
ノート
印刷プレビュー

反応式

HRID 420971 の反応式
[Na+].[I-:2].ClN1C(=O)CCC1=O.[CH2:11]([O:13][C:14]([C:16]1[NH:17][C:18]2[C:23]([CH:24]=1)=[CH:22][C:21]([C:25]1[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:33])[F:32])=[CH:27][CH:26]=1)=[CH:20][CH:19]=2)=[O:15])[CH3:12].[O-]S([O-])(=S)=O.[Na+].[Na+]>CC(C)=O>[CH2:11]([O:13][C:14]([C:16]1[NH:17][C:18]2[C:23]([C:24]=1[I:2])=[CH:22][C:21]([C:25]1[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:32])[F:33])=[CH:27][CH:26]=1)=[CH:20][CH:19]=2)=[O:15])[CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 5238Sodium IodideHCID 24477Sodium ThiosulfateHCID 31398ChlorosuccinimideHCID 57419913Ethyl 5-(4-(trifluoromethyl)phenyl)-1H-indole-2-carboxylate

生成物 1

HCID 574199143-Iodo-5-(4-trifluoromethylphenyl)indole-2-carboxylic acid ethyl ester

試薬・触媒・溶媒 1

HCID 180
Acetone
溶媒
3 回

実験手順

NaI (2.04 g, 14 mmol) in acetone (10 mL) was added dropwise to a stirred solution of N-chlorosuccinimide (1.83 g, 14 mmol) in acetone (10 mL) protected from light. After 15 min, a solution of 5-(4-trifluoromethylphenyl)indole-2-carboxylic acid ethyl ester (3.80 g, 11 mmol; see step (a) above) in acetone (60 mL) was added dropwise, followed by stirring for 2 h at rt. The mixture was poured into Na2S2O3 (aq, 10%, 250 mL) and extracted with EtOAc (200 mL). The combined extracts were washed with NaHCO3 (aq, sat), water and brine, dried (Na2SO4) and concentrated. The residue was treated with petroleum ether to give the sub-title compound. Yield 4.88 g (93%).

後処理

  1. extractionextracted with EtOAc (200 mL)
  2. washThe combined extracts were washed with NaHCO3 (aq, sat), water and brine
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated
  5. additionThe residue was treated with petroleum ether

出典と根拠

ORDレコード
ord-2726ce31a1a94c6d992276d562473f9f
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08097623B2

反応ノート

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