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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Carbonate → 4-(2-Methoxyethyl)piperazine-1-carbaldehyde

HRID 1740380
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HRID 1740380 반응식
[CH:1]([N:3]1[CH2:8][CH2:7][NH:6][CH2:5][CH2:4]1)=[O:2].C(=O)([O-])[O-].[Na+].[Na+].[CH3:15][O:16][CH2:17][CH2:18]Br>CO>[CH:1]([N:3]1[CH2:8][CH2:7][N:6]([CH2:18][CH2:17][O:16][CH3:15])[CH2:5][CH2:4]1)=[O:2]
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참가 물질

5

반응물 3

HCID 10340Sodium CarbonateHCID 809722-Bromoethyl methyl etherHCID 821911-Piperazinecarboxaldehyde

생성물 1

HCID 218386494-(2-Methoxyethyl)piperazine-1-carbaldehyde수율 102.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 37.1 g of N-formylpiperazine and 37.1 g of anhydrous sodium carbonate in 50 mL of methanol was added dropwise 53.15 g of methoxyethyl bromide, and the mixture was refluxed for 3.5 hours. After cooling to room temperature, insolubles were filtered out and the filtrate was concentrated. To the residue was added water and chloroform. After separating the organic layer, the aqueous layer was extracted with chloroform. The combined organic layer was dried over anhydrous magnesium sulfate and concentrated to give 57.2 g of the title compound.

후처리

  1. temperaturethe mixture was refluxed for 3.5 hours
  2. filtrationinsolubles were filtered out
  3. concentrationthe filtrate was concentrated
  4. additionTo the residue was added water and chloroform
  5. customAfter separating the organic layer
  6. extractionthe aqueous layer was extracted with chloroform
  7. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-aaaf1bfb69a940fe969a8ee59137fee5
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05969138

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