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Methyl 5-bromoindoline-7-carboxylate → methyl 5-bromo-1H-indole-7-carboxylate

HRID 656005
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HRID 656005 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:11]([O:13][CH3:14])=[O:12])[CH:10]=1)[NH:7][CH2:6][CH2:5]2>O1CCCC1.[O-2].[O-2].[Mn+4]>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:11]([O:13][CH3:14])=[O:12])[CH:10]=1)[NH:7][CH:6]=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 49758858Methyl 5-bromoindoline-7-carboxylate

생성물 1

HCID 24728848methyl 5-bromo-1H-indole-7-carboxylate수율 80.3%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매2회HCID 8028Tetrahydrofuran용매

실험 절차

Methyl 5-bromo-2,3-dihydro-1H-indole-7-carboxylate (6.5 g, 25 mmol) was dissolved in tetrahydrofuran (100 mL). Activated manganese dioxide (5 μm particle size, 22 g, 250 mmol) was added and the mixture stirred at room temperature for 16 hours. A further 22 g of activated manganese dioxide was added and the reaction stirred for 96 hours. The reaction was then filtered through celite and concentrated in vacuo to give 5.1 g (80%) of the title compound as a beige solid.

후처리

  1. stirringthe reaction stirred for 96 hours
  2. filtrationThe reaction was then filtered through celite and
  3. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-92feb91ec1944631b25b642e80d6f1d2
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071584B2

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