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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-bromobutanimide → 5-Bromo-4,6-difluoroindoline

HRID 338228
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HRID 338228 반응식
[F:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][NH:6]2.[Br:12]N1C(=O)CCC1=O>C(#N)C>[Br:12][C:10]1[C:2]([F:1])=[C:3]2[C:7](=[CH:8][C:9]=1[F:11])[NH:6][CH2:5][CH2:4]2
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 162444494,6-Difluoro-2,3-dihydro-1H-indole

생성물 1

HCID 838958425-Bromo-4,6-difluoroindoline수율 83%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of 4,6-difluoroindoline (4.6 g, 29.8 mmol) in acetonitrile (50 mL) was added a solution of N-bromosuccinimide (3.68 g, 20.6 mmol) acetonitrile (30 mL) at 0° C. dropwise. The reaction was stirred for 30 minutes and quenched with saturated aqueous sodium bicarbonate solution and diluted with ethyl acetate. The layers were separated and the organic phases were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (0-60% ethyl acetate in petroleum ether) to give the title compound (4.0 g, 58% yield) as colorless oil

후처리

  1. customquenched with saturated aqueous sodium bicarbonate solution
  2. additiondiluted with ethyl acetate
  3. customThe layers were separated
  4. dry with materialthe organic phases were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flash chromatography (0-60% ethyl acetate in petroleum ether)

출처 및 근거

ORD 기록
ord-3c79293afe6a4d389402c07a59cecca4
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889730B2

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