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Water → 1-Oleoylpiperazine

HRID 892889
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HRID 892889 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 4837PiperazineHCID 53677849-Octadecene, 1-chloro-

생성물 1

HCID 677939691-Oleoylpiperazine수율 76%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-e9f128aba7b84a5bb177cc6ad75977e9
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05120738

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