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Water → N-[3-(carbamothioylamino)phenyl]acetamide

HRID 2086763
ノート
印刷プレビュー

反応式

HRID 2086763 の反応式
[S-:1][C:2]#[N:3].[NH4+].C(Cl)(=O)C1C=CC=CC=1.[NH2:14][C:15]1[CH:16]=[C:17]([CH:22]=[CH:23][CH:24]=1)[NH:18][C:19](=[O:21])[CH3:20].O>CC(C)=O>[C:19]([NH:18][C:17]1[CH:16]=[C:15]([NH:14][C:2]([NH2:3])=[S:1])[CH:24]=[CH:23][CH:22]=1)(=[O:21])[CH3:20]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 7412Benzoyl chlorideHCID 7604m-AminoacetanilideHCID 15666Ammonium thiocyanate

生成物 1

HCID 6451295N-[3-(carbamothioylamino)phenyl]acetamide収率 60.6%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒2 回

反応条件

温度
50 °C

実験手順

A mixture of ammonium thiocyanate (2.79 g) and benzoyl chloride (3.86 ml) in acetone (30 ml) was refluxed for 5 minutes. Then a solution of 3′-aminoacetanilide (5.00 g) in acetone (40 ml) was added thereto. The mixture was poured into water, and the resulting precipitate was separated by filtration. The crystals were heated at 50° C. for 3 hours with 1N sodium hydroxide (150 ml) solution. The mixture was poured into a mixture of ethyl acetate and water, and the resulting precipitate was collected and washed with ethyl acetate and water to give N-(3-acetylaminophenyl)thiourea (4.22 g).

後処理

  1. temperaturewas refluxed for 5 minutes
  2. customthe resulting precipitate was separated by filtration
  3. additionThe mixture was poured into a mixture of ethyl acetate and water
  4. customthe resulting precipitate was collected
  5. washwashed with ethyl acetate and water

出典と根拠

ORDレコード
ord-68ab111ee64c44509f20a3bcbfcbff33
出典データセット
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06727245B2

反応ノート

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