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N-Iodosuccinimide → 7-Iodo-4-(trifluoromethyl)-1H-indole-2,3-dione

HRID 1369082
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HRID 1369082 반응식
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:4]=1[C:5](=[O:13])[C:6](=[O:12])[NH:7]2.[I:16]N1C(=O)CCC1=O>OS(O)(=O)=O>[I:16][C:9]1[CH:10]=[CH:11][C:3]([C:2]([F:1])([F:14])[F:15])=[C:4]2[C:8]=1[NH:7][C:6](=[O:12])[C:5]2=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 120273N-IodosuccinimideHCID 126294174-(Trifluoromethyl)-1H-indole-2,3-dione

생성물 1

HCID 185185657-Iodo-4-(trifluoromethyl)-1H-indole-2,3-dione수율 42%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

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온도
40 °C

실험 절차

A mixture of 4-trifluoromethylisatin (450 mg, 2.09 mmol) and N-iodosuccinimide (800 mg, 3.72 mmol) in conc. H2SO4 (5 mL) was stirred for 6 h at 40° C. and poured into crushed ice. The mixture was extracted with ethyl acetate and the extracts were washed with aqueous Na2SO3, dried over MgSO4, and concentrated. The residue was purified by silica gel column chromatography with 3:1 hexane/ethyl acetate to give the title compound (296 mg, 42%).

후처리

  1. additionpoured
  2. custominto crushed ice
  3. extractionThe mixture was extracted with ethyl acetate
  4. washthe extracts were washed with aqueous Na2SO3
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel column chromatography with 3:1 hexane/ethyl acetate

출처 및 근거

ORD 기록
ord-200d528cbf4d4f4faa879521d7acd9e1
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06576656B1

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