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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Sulfuric Acid → HCID 21873086、化合物

HRID 614865
ノート
印刷プレビュー

反応式

HRID 614865 の反応式
[Cl:1][CH2:2][C:3]#[N:4].[Cl:5][C:6]([Cl:19])([Cl:18])[CH:7](O)[NH:8][C:9](=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.S(=O)(=O)(O)[OH:21]>>[Cl:5][C:6]([Cl:19])([Cl:18])[CH:7]([NH:8][C:9](=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[NH:4][C:3](=[O:21])[CH2:2][Cl:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 1118Sulfuric AcidHCID 7856ChloroacetonitrileHCID 39323N-(2,2,2-trichloro-1-hydroxyethyl)benzamide

生成物 1

HCID 21873086HCID 21873086、化合物

実験手順

Chloroacetonitrile (4.1g) was added dropwise to a solution of 1,1,1-trichloro-2-hydroxy-2-benzamidoethane (13.4g) in concentrated sulphuric acid (50 ml). The temperature was kept at 0° during the addition. The mixture was stirred at room temperature for 4 hours, then left overnight. The reaction mixture was poured on to ice. The precipitated solid was collected, washed with water and dried (14.65g). Recrystallisation from nitromethane gave pure 1,1,1-trichloro-2-benzamido-2-(chloroacetamido)ethane (12.7g, m.p. 210°-12°) whose infra red spectrum was identical to that of the product of the preceding Example.

後処理

  • additionThe temperature was kept at 0° during the addition
  • waitleft overnight
  • additionThe reaction mixture was poured on to ice
  • customThe precipitated solid was collected
  • washwashed with water
  • customdried (14.65g)
  • customRecrystallisation from nitromethane
  • 出典と根拠

    ORDレコード
    ord-5ae4b272ea484b8a8dfd91e618d5b1b1
    出典データセット
    uspto-grants-1979_03
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04146646

    反応ノート

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