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Methyl iodide → HCID 59463819, 화합물

HRID 1713399
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인쇄 미리보기

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HRID 1713399 반응식
[Br:1][C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[C:5](=[O:12])[NH:4][CH:3]=1.[CH3:13]I>C(Cl)(Cl)Cl.C(=O)([O-])[O-].[Ag+].[Ag+]>[Br:1][C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[C:5]([O:12][CH3:13])=[N:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6328Methyl iodideHCID 594638144-bromo-5,6,7,8-tetrahydro-1(2H)-Isoquinolinone

생성물 1

HCID 59463819HCID 59463819, 화합물수율 84%

시약·촉매·용매 2

HCID 92796Silver carbonate촉매HCID 6212Chloroform용매

반응 조건

온도
50 °C

실험 절차

47.7 g (209 mmol) of 4-bromo-5,6,7,8-tetrahydro-2H-isoquinolin-1-one are dissolved in 1 l of chloroform and, after addition of 77.8 g (282 mmol) of silver(I) carbonate and 53.5 ml (118.7 g, 836 mmol) of methyl iodide, stirred at 50° C. for 3 h. After cooling, the suspension is filtered through Celite, concentrated and chromatographed on silica gel using n-heptane with addition of 2% ethyl acetate. A colorless oil (42.5 g, 84% yield) is obtained.

후처리

  1. temperatureAfter cooling
  2. filtrationthe suspension is filtered through Celite
  3. concentrationconcentrated
  4. customchromatographed on silica gel
  5. additionwith addition of 2% ethyl acetate

출처 및 근거

ORD 기록
ord-7fb22eb221004955a6bad02614f70010
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07795278B2

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