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Water → (1-Methyl-6-nitro-1H-indol-3-yl)-acetonitrile

HRID 1004208
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HRID 1004208 반응식
C(=O)([O-])[O-].[K+].[K+].[N+:7]([C:10]1[CH:18]=[C:17]2[C:13]([C:14]([CH2:19][C:20]#[N:21])=[CH:15][NH:16]2)=[CH:12][CH:11]=1)([O-:9])=[O:8].[CH3:22]I.O>CN(C)C=O>[CH3:22][N:16]1[C:17]2[C:13](=[CH:12][CH:11]=[C:10]([N+:7]([O-:9])=[O:8])[CH:18]=2)[C:14]([CH2:19][C:20]#[N:21])=[CH:15]1
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참가 물질

6

반응물 4

HCID 962WaterHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 2523851h-Indole-3-acetonitrile, 6-nitro-

생성물 1

HCID 21999030(1-Methyl-6-nitro-1H-indol-3-yl)-acetonitrile수율 98.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

65.5 g (0.474 mol) of powdered potassium carbonate was added to a solution of 28.9 g (0.143 mol) of (6-nitro-1H-indol-3,yl)-acetonitrile (13) from Step C above in 230 ml of dimethylformamide at room temperature. The suspension was stirred for 40 minutes then 25.48 g (0.179 mol) of methyl iodide was added dropwise over 65 minutes. After stirring at room temperature over night the reaction mixture was cooled and poured into a total of 600 ml of water. The precipitate was filtered, washed with a little water and dried on phosphor anhydride until reaching constant weight. The procedure yielded 30.4 g (95.4%) of (1-methyl-6-nitro-1H-indol-3-yl)acetonitrile (14), which was used without further purification.

후처리

  1. stirringAfter stirring at room temperature over night the reaction mixture
  2. temperaturewas cooled
  3. filtrationThe precipitate was filtered
  4. washwashed with a little water
  5. dry with materialdried on phosphor anhydride

출처 및 근거

ORD 기록
ord-9b1f4588515e487bb45d15caee771637
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06048887

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