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Ethyl Acrylate → N-[1-(ethoxycarbonylethyl)-piperid-4-yl]-N-methylpropionamide

HRID 2082358
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인쇄 미리보기

반응식

HRID 2082358 반응식
[NH:1]1[CH2:6][CH2:5][CH:4]([N:7]([CH3:12])[C:8](=[O:11])[CH2:9][CH3:10])[CH2:3][CH2:2]1.[C:13]([O:17][CH2:18][CH3:19])(=[O:16])[CH:14]=[CH2:15]>C(O)C>[CH2:18]([O:17][C:13]([CH2:14][CH2:15][N:1]1[CH2:6][CH2:5][CH:4]([N:7]([CH3:12])[C:8](=[O:11])[CH2:9][CH3:10])[CH2:3][CH2:2]1)=[O:16])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8821Ethyl AcrylateHCID 19761222N-Methyl-N-(piperidin-4-yl)propionamide

생성물 1

HCID 19761283N-[1-(ethoxycarbonylethyl)-piperid-4-yl]-N-methylpropionamide

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

7.4 g of the compound obtained in Stage C of Example 1 are dissolved in 10 ml of ethanol, then 4.73 ml of ethyl acrylate dissolved in 12 ml of ethanol are poured onto the solution. The mixture is left at room temperature for one night, and then concentrated in a rotary evaporator and distilled in a Kugelrohr to yield the compound in the form of an oil.

후처리

  1. additionare poured onto the solution
  2. waitThe mixture is left at room temperature for one night
  3. concentrationconcentrated in a rotary evaporator
  4. distillationdistilled in a Kugelrohr
  5. customto yield the compound in the form of an oil

출처 및 근거

ORD 기록
ord-a719ef78986d43f6a1540eae9e37334b
출처 데이터셋
uspto-grants-1993_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05189045

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