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Acetic Acid → Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylate

HRID 706974
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인쇄 미리보기

반응식

HRID 706974 반응식
N1([CH:7]=[C:8]2[CH2:13][CH2:12][N:11]([C:14]([O:16][CH2:17][C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[O:15])[CH2:10][CH2:9]2)CCCCC1.[CH3:24][C:25](=[O:28])[CH:26]=[CH2:27].C(O)(=O)C>C(O)C>[O:28]=[C:25]1[CH2:24][CH2:7][C:8]2([CH2:9][CH2:10][N:11]([C:14]([O:16][CH2:17][C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)=[O:15])[CH2:12][CH2:13]2)[CH:27]=[CH:26]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 6570Methyl vinyl ketoneHCID 86642880Benzyl 4-(piperidin-1-ylmethylene)piperidine-1-carboxylate

생성물 1

HCID 23435732Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of EXAMPLE 265A (15.88 g) in ethanol (300 mL) was added but-3-enone (3.89 g). The mixture was stirred at reflux overnight. Then acetic acid (30 mL) was added to the mixture which was stirred at reflux again overnight. The mixture was then concentrated under vacuum and the residue was diluted with ethyl acetate (400 mL) and washed with water and brine and dried over Na2SO4. After filtration and evaporation of the solvent, column purification gave the title compound.

후처리

  1. temperatureat reflux overnight
  2. stirringwas stirred
  3. temperatureat reflux again overnight
  4. concentrationThe mixture was then concentrated under vacuum
  5. additionthe residue was diluted with ethyl acetate (400 mL)
  6. washwashed with water and brine
  7. dry with materialdried over Na2SO4
  8. filtrationAfter filtration and evaporation of the solvent, column purification

출처 및 근거

ORD 기록
ord-328bc85cbaa647f8894a94b9c7946c5d
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09174982B2

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