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Sodium Hydroxide → 3-chloro-N-[3-(1H-imidazol-1-yl)propyl]benzamide

HRID 1589174
ノート
印刷プレビュー

反応式

HRID 1589174 の反応式
Cl.Cl.[N:3]1([CH2:8][CH2:9][CH2:10][NH2:11])[CH:7]=[CH:6][N:5]=[CH:4]1.[OH-].[Na+].[Cl:14][C:15]1[CH:16]=[C:17]([CH:21]=[CH:22][CH:23]=1)[C:18](Cl)=[O:19]>C(Cl)Cl>[Cl:14][C:15]1[CH:16]=[C:17]([CH:21]=[CH:22][CH:23]=1)[C:18]([NH:11][CH2:10][CH2:9][CH2:8][N:3]1[CH:7]=[CH:6][N:5]=[CH:4]1)=[O:19]
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 14798Sodium Hydroxide2 回HCID 69252Benzoyl chloride, 3-chloro-HCID 122509693-(Imidazole-1-yl)-propylamine Dihydrochloride

生成物 1

HCID 28482203-chloro-N-[3-(1H-imidazol-1-yl)propyl]benzamide

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A mixture of 6.0 g. of 1H-imidazole-1-propanamine dihydrochloride, 45 ml. of 2N sodium hydroxide and 150 ml. of methylene chloride was stirred at room temperature and 3.9 ml. of 3-chlorobenzoyl chloride was added. The reaction mixture was stirred for 18 hours, then methylene chloride and 15 ml. of 1N sodium hydroxide were added and the layers were separated. The organic layer was washed with water, dried over magnesium sulfate, and concentrated to remove the solvent. The residue was triturated with diethyl ether and the crystalline product recovered by filtration and recrystallized from ethanol, giving the desired product, m.p. 125°-127° C.

後処理

  1. additionA mixture of 6.0 g
  2. customthe layers were separated
  3. washThe organic layer was washed with water
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customto remove the solvent
  7. customThe residue was triturated with diethyl ether
  8. filtrationthe crystalline product recovered by filtration
  9. customrecrystallized from ethanol

出典と根拠

ORDレコード
ord-e7a99a1e55744f3d8b8b83b92d1c4af8
出典データセット
uspto-grants-1986_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04568687

反応ノート

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