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Methyl iodide → 1,1'-(9-methyl-9H-carbazole-2,7-diyl)diethanone

HRID 337393
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인쇄 미리보기

반응식

HRID 337393 반응식
I[CH3:2].[CH:3]1[C:15]2[NH:14][C:13]3[C:8](=[CH:9][CH:10]=[C:11]([C:16](=[O:18])[CH3:17])[CH:12]=3)[C:7]=2[CH:6]=[CH:5][C:4]=1[C:19](=[O:21])[CH3:20].[OH-].[K+]>C1COCC1>[CH3:2][N:14]1[C:13]2[CH:12]=[C:11]([C:16](=[O:18])[CH3:17])[CH:10]=[CH:9][C:8]=2[C:7]2[C:15]1=[CH:3][C:4]([C:19](=[O:21])[CH3:20])=[CH:5][CH:6]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 14797Potassium HydroxideHCID 42891861-(7-acetyl-9H-carbazol-2-yl)ethanone

생성물 1

HCID 578167421,1'-(9-methyl-9H-carbazole-2,7-diyl)diethanone

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Iodomethane (0.747 mL, 11.94 mmol) was added to the mixture of 1,1′-(9H-carbazole-2,7-diyl)diethanone (1 g, 3.98 mmol) and potassium hydroxide (0.223 g, 3.98 mmol) in THF (20 mL) and stirred for overnight at room temperature. The solvent was then removed under reduced pressure and the crude was extracted with dichloromethane and washed with water. The organic layer was dried over Na2SO4 and evaporated to get the pure product as yellow solid.

후처리

  1. customThe solvent was then removed under reduced pressure
  2. extractionthe crude was extracted with dichloromethane
  3. washwashed with water
  4. dry with materialThe organic layer was dried over Na2SO4
  5. customevaporated

출처 및 근거

ORD 기록
ord-669e81930024469bbda6dc5d392c71c8
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889726B2

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