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Piperazine → 1-[4-(Propan-2-yl)piperazin-1-yl]ethan-1-one

HRID 1003320
ノート
印刷プレビュー

反応式

HRID 1003320 の反応式
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[I-].[Na+].[C:9](=[O:12])([O-])[O-].[K+].[K+].Br[CH:16]([CH3:18])[CH3:17].[CH:19](Cl)(Cl)Cl>CO>[C:9]([N:1]1[CH2:6][CH2:5][N:4]([CH:16]([CH3:18])[CH3:17])[CH2:3][CH2:2]1)(=[O:12])[CH3:19]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 4837PiperazineHCID 5238Sodium IodideHCID 6212ChloroformHCID 63582-BromopropaneHCID 11430Potassium Carbonate

生成物 1

HCID 187964191-[4-(Propan-2-yl)piperazin-1-yl]ethan-1-one

試薬・触媒・溶媒 1

HCID 887
Methanol
溶媒

反応条件

温度
60 °C

実験手順

To 12.95 g of piperazine, 0.75 g of sodium iodide and 3.46 g of potassium carbonate were added successively 25 ml of methanol and 6.15 g of 2-bromopropane and the mixture was stirred at 60° C. for 4 hours. After the addition of chloroform and washing with a saturated aqueous solution of sodium chloride, the mixture was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, 12 ml of acetic anhydride was slowly added and the mixture was stirred at room temperature for 2.5 hours. The reaction solution was poured into ice and chloroform was added and the mixture was neutralized with sodium carbonate. After extracting with chloroform, the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue thus obtained was chromatographed over a silica gel column. The solvent was distilled off and the residue was allowed to stand overnight. The diacetylpiperazine thus precipitated out was filtered off to afford 7.26 g of the title compound as an oily substance.

後処理

  1. washwashing with a saturated aqueous solution of sodium chloride
  2. dry with materialthe mixture was dried over anhydrous magnesium sulfate
  3. distillationThe solvent was distilled off under reduced pressure, 12 ml of acetic anhydride
  4. additionwas slowly added
  5. stirringthe mixture was stirred at room temperature for 2.5 hours
  6. additionThe reaction solution was poured into ice and chloroform
  7. additionwas added
  8. extractionAfter extracting with chloroform
  9. dry with materialthe extract was dried over anhydrous magnesium sulfate
  10. distillationThe solvent was distilled off under reduced pressure
  11. customthe residue thus obtained
  12. customwas chromatographed over a silica gel column
  13. distillationThe solvent was distilled off
  14. waitto stand overnight
  15. customThe diacetylpiperazine thus precipitated out
  16. filtrationwas filtered off

出典と根拠

ORDレコード
ord-ab004de9e77242eeaf0b66d58115bfd2
出典データセット
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06046201

反応ノート

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