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

HRID 420971
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HRID 420971 반응식
[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]
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참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 180
Acetone
용매
3회

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-2726ce31a1a94c6d992276d562473f9f
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08097623B2

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