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Acetyl chloride → HCID 22751286、化合物

HRID 2163677
ノート
印刷プレビュー

反応式

HRID 2163677 の反応式
[C:1]1([CH:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:8][C:9]2[NH:10][CH2:11][CH2:12][N:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:20](Cl)(=[O:22])[CH3:21]>N1C=CC=CC=1>[C:20]([N:13]1[CH2:12][CH2:11][N:10]=[C:9]1[CH2:8][CH:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)(=[O:22])[CH3:21]
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 2

HCID 6367Acetyl chlorideHCID 12632114HCID 12632114、化合物

生成物 1

HCID 22751286HCID 22751286、化合物

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒2 回

実験手順

To a mixture of 5.0 g of 2-(2,2-diphenyl ethyl)-2-imidazoline and 50 ml of pyridine, 1.1 g of acetyl chloride was dropwise added and the solution stirred at room temperature for about 2 hours. After the reaction, pyridine was removed by distillation. To the resulting residue there was added 100 ml of benzene and the same amount of water, and the solution was well shaken. The benzene layer was separated, washed with water and dried with sodium sulfate. After removing benzene from the solution, the resulting residue was recrystallized from ether to give 1-acetyl-2-(2,2-diphenyl ethyl)-2-imidazoline having a melting point of 104°-106° C.

後処理

  1. additionwas dropwise added
  2. customwas removed by distillation
  3. additionTo the resulting residue there was added 100 ml of benzene
  4. stirringthe same amount of water, and the solution was well shaken
  5. customThe benzene layer was separated
  6. washwashed with water
  7. dry with materialdried with sodium sulfate
  8. customAfter removing benzene from the solution
  9. customthe resulting residue was recrystallized from ether

出典と根拠

ORDレコード
ord-c656a6251b0845a2823a41f00b03aa00
出典データセット
uspto-grants-1979_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04136188

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート