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1-Piperazinecarboxaldehyde → HCID 19421679、化合物

HRID 743036
ノート
印刷プレビュー

反応式

HRID 743036 の反応式
C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.[CH:18]([N:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1)=[O:19].[CH3:26][O:27][C:28]1[CH:33]=[CH:32][C:31]([C:34]([C:39]2[CH:44]=[CH:43][C:42]([O:45][CH3:46])=[CH:41][CH:40]=2)=[CH:35]C(O)=O)=[CH:30][CH:29]=1.C(=O)(O)[O-].[Na+]>C(N(CC)CC)C.C(Cl)Cl>[CH3:46][O:45][C:42]1[CH:41]=[CH:40][C:39]([C:34]([C:31]2[CH:30]=[CH:29][C:28]([O:27][CH3:26])=[CH:33][CH:32]=2)=[CH:35][C:18]([N:20]2[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]2)=[O:19])=[CH:44][CH:43]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 821911-PiperazinecarboxaldehydeHCID 199401P,P-Diphenylphosphinic azideHCID 516892Sodium BicarbonateHCID 12660800HCID 12660800、化合物

生成物 1

HCID 19421679HCID 19421679、化合物

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒
HCID 8471
Triethylamine
溶媒

実験手順

3,41 ml of diphenylphosphoryl azide and 1.09 ml of 1-formylpiperazine were added to a 60 ml of a methylene chloride solution of 3.00 g of 3,3-bis(4-methoxyphenyl)acrylic acid and 2.94 ml of triethylamine. The reaction mixture was then stirred for2 hours at room temperature, after which it was poured into a saturated aqueous solution of sodium bicarbonate and extracted twice with methylene chloride. The combined extracts were washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was dissolved in 80 ml of methanol, and 40 ml of a 10% w/v aqueous solution of sodium hydroxide were added to the resulting solution. The reaction mixture was stirred for 18 hours at room temperature and then poured into water: it was then extracted twice with methylene chloride. The combined extracts were washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography through 80 g of silica gel eluted with mixtures of methylene chloride and methanol ranging from 19:1 to 4:1 by volume to give 3.00 g of 1-[3,3-bis(4-methoxyphenyl)acryloyl]piperazine as a powder.

後処理

  1. extractionextracted twice with methylene chloride
  2. washThe combined extracts were washed with water
  3. dry with materialdried over anhydrous sodium sulfate
  4. customevaporated under reduced pressure
  5. dissolutionThe residue was dissolved in 80 ml of methanol
  6. addition40 ml of a 10% w/v aqueous solution of sodium hydroxide were added to the resulting solution
  7. stirringThe reaction mixture was stirred for 18 hours at room temperature
  8. additionpoured into water
  9. extractionit was then extracted twice with methylene chloride
  10. washThe combined extracts were washed with water
  11. dry with materialdried over anhydrous sodium sulfate
  12. customevaporated under reduced pressure
  13. customThe residue was purified by column chromatography through 80 g of silica gel
  14. washeluted with mixtures of methylene chloride and methanol ranging from 19:1 to 4:1 by volume

出典と根拠

ORDレコード
ord-e3b92833b9c2462b94a215b78ef46c8d
出典データセット
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05556852

反応ノート

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