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Methyl iodide → HCID 550302, 화합물

HRID 732087
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HRID 732087 반응식
[CH3:1][NH:2][C:3](=[S:6])[NH:4][NH2:5].[CH3:7]I.[C:9](O)([C:11]([F:14])([F:13])[F:12])=O>CCO>[CH3:1][N:2]1[C:9]([C:11]([F:14])([F:13])[F:12])=[N:5][N:4]=[C:3]1[S:6][CH3:7]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 6422Trifluoroacetic acidHCID 2723853N-Methylhydrazinecarbothioamide

생성물 1

HCID 550302HCID 550302, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

4-Methylthiosemicarbazid (10.0 g, 95.09 mmol) in TFA (46.7 ml) was heated to reflux o.n. Excess TFA was removed via evaporation. The residue was dissolved in aq. 1M NaOH (100 ml), followed by dropwise addition of CH3I (4.47 ml, 71.17 mmol) in EtOH (22 ml). The resulting mixture was stirred o.n. Partial evaporation of the solvent induced crystallization. After dilution with H2O the solid was collected via filtration and gave after drying the title compound (5.2 g, 28%). MS (M++1) 198

후처리

  1. temperatureto reflux o.n
  2. customExcess TFA was removed via evaporation
  3. dissolutionThe residue was dissolved in aq. 1M NaOH (100 ml)
  4. customPartial evaporation of the solvent induced crystallization
  5. filtrationAfter dilution with H2O the solid was collected via filtration
  6. customgave
  7. dry with materialafter drying the title compound (5.2 g, 28%)

출처 및 근거

ORD 기록
ord-c4bd093d6b4e4b9da1c1cef9a95e38fe
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07585881B2

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