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Methyl iodide → HCID 550302、化合物

HRID 732087
ノート
印刷プレビュー

反応式

HRID 732087 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 6422Trifluoroacetic acidHCID 2723853N-Methylhydrazinecarbothioamide

生成物 1

HCID 550302HCID 550302、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

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

後処理

  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%)

出典と根拠

ORDレコード
ord-c4bd093d6b4e4b9da1c1cef9a95e38fe
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07585881B2

反応ノート

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