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Water → 1-Oleoylpiperazine

HRID 892889
ノート
印刷プレビュー

反応式

HRID 892889 の反応式
[CH2:1](Cl)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[NH:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1.[OH2:26]>C(Cl)Cl>[C:1]([N:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1)(=[O:26])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]
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 962WaterHCID 4837PiperazineHCID 53677849-Octadecene, 1-chloro-

生成物 1

HCID 677939691-Oleoylpiperazine収率 76%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of 3.0 g of oleyl chloride in 10 mg of methylene chloride was added portion-wise to a solution of 4.3 g of piperazine in 30 ml of methylene chloride with stirring under ice cooling. After stirring the mixture in situ for additional 2 hours, 10 ml of water was added to the reaction mixture to separate the organic layer. The organic layer was further washed with water and dried over anhydrous sodium sulfate, followed by removal of the solvent by evaporation. The residue obtained was purified by silica gel column chromatography to obtain 2.68 g of the objective compound (yield: 76%).

後処理

  1. stirringAfter stirring the mixture in situ for additional 2 hours
  2. customto separate the organic layer
  3. washThe organic layer was further washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. customfollowed by removal of the solvent by evaporation
  6. customThe residue obtained
  7. customwas purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-e9f128aba7b84a5bb177cc6ad75977e9
出典データセット
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05120738

反応ノート

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