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Sodium Hydroxide → 3-Ethyl-3-(3-nitrophenyl)-4-pentenoic acid

HRID 397747
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HRID 397747 반응식
[CH2:1]([C:3]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=1)([CH:9]=[CH2:10])[CH2:4][C:5]([O:7]C)=[O:6])[CH3:2].[OH-].[Na+]>C(O)(C)C>[CH2:9]([C:3]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=1)([CH:1]=[CH2:2])[CH2:4][C:5]([OH:7])=[O:6])[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 23000907Methyl 3-ethyl-3-(3-nitrophenyl)-4-pentenoate

생성물 1

HCID 230010243-Ethyl-3-(3-nitrophenyl)-4-pentenoic acid

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

A solution of methyl 3-ethyl-3-(3-nitrophenyl)-4-pentenoate (Preparation 59, assume 7.25 mmol) in isopropyl alcohol (9 ml) and 2M aqueous sodium hydroxide solution (4.4 ml, 8.75 mmol) was heated under reflux for 11 h, then the reaction mixture was concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The phases were separated and the organic extract was dried (MgSO4), filtered and concentrated in vacuo to give the title compound as an oil which was used without further purification.

후처리

  1. temperatureunder reflux for 11 h
  2. concentrationthe reaction mixture was concentrated in vacuo
  3. customThe residue was partitioned between ethyl acetate and water
  4. customThe phases were separated
  5. extractionthe organic extract
  6. dry with materialwas dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-89ff49498f134b0d84c637c9dce5d122
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06610711B2

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