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Carbon Disulfide → 5-Chloro-6-iodo-1H-benzo[d]imidazole-2(3H)-thione

HRID 340765
ノート
印刷プレビュー

反応式

HRID 340765 の反応式
[OH-].[K+].[C:3](=[S:5])=S.[Cl:6][C:7]1[CH:8]=[C:9]([NH2:15])[C:10]([NH2:14])=[CH:11][C:12]=1[I:13]>O.CCO>[Cl:6][C:7]1[C:12]([I:13])=[CH:11][C:10]2[NH:14][C:3](=[S:5])[NH:15][C:9]=2[CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6348Carbon DisulfideHCID 14797Potassium HydroxideHCID 574814674-Chloro-5-iodobenzene-1,2-diamine

生成物 1

HCID 574814685-Chloro-6-iodo-1H-benzo[d]imidazole-2(3H)-thione

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

KOH (15.7 g, 238 mmol) in water (50 mL), followed by carbon disulfide (14.4 mL, 238 mmol), was added to a solution of 4-chloro-5-iodobenzene-1,2-diamine (50 g, 198 mmol) in EtOH (300 mL). The mixture was heated at reflux for 3 h, cooled and filtered. To the filtrate was added water (300 mL) and then AcOH (25 mL) in water (50 mL). The resulting precipitate was collected, washed with water and a small amount of EtOH, and then dried to afford the desired product as a brown powder, which was used in the next step without further purification.

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 3 h
  3. temperaturecooled
  4. filtrationfiltered
  5. additionTo the filtrate was added water (300 mL)
  6. customThe resulting precipitate was collected
  7. washwashed with water
  8. dry with materiala small amount of EtOH, and then dried

出典と根拠

ORDレコード
ord-5a0e54d45a22476889bb42ebe2729721
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895596B2

反応ノート

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