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1-Piperazinecarboxaldehyde → HCID 19421679, 화합물

HRID 744088
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HRID 744088 반응식
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
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참가 물질

7

반응물 4

HCID 821911-PiperazinecarboxaldehydeHCID 199401P,P-Diphenylphosphinic azideHCID 516892Sodium BicarbonateHCID 12660800HCID 12660800, 화합물

생성물 1

HCID 19421679HCID 19421679, 화합물

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 8471
Triethylamine
용매

실험 절차

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 for 2 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.

후처리

  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

출처 및 근거

ORD 기록
ord-cda698af916d453a83a4cef4817bb5b9
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05559109

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