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Lithium Hydroxide → Cgs 22745

HRID 2371968
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HRID 2371968 반응식
[CH3:1][C:2]1[N:3]([C:8]2[CH:13]=[CH:12][C:11](/[CH:14]=[CH:15]/[C:16]([N:18]([O:20]C(=O)C)[CH3:19])=[O:17])=[CH:10][CH:9]=2)[C:4]([CH3:7])=[CH:5][CH:6]=1.[OH-].[Li+]>CC(O)C>[CH3:1][C:2]1[N:3]([C:8]2[CH:13]=[CH:12][C:11](/[CH:14]=[CH:15]/[C:16]([N:18]([OH:20])[CH3:19])=[O:17])=[CH:10][CH:9]=2)[C:4]([CH3:7])=[CH:5][CH:6]=1
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참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 19905480HCID 19905480, 화합물

생성물 1

HCID 6439321Cgs 22745

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

To a solution of 3.12 g (E)-3-[4-(2,5-dimethyl-1-H-pyrrol-1-yl)phenyl]-N-acetoxy-N-methyl-2-propenamide in 2-propanol (50 ml) cooled to 0°, 1N aqueous lithium hydroxide (13 ml) is added with stirring. The mixture is stirred at room temperature for 30 minutes, then partitioned between ethyl acetate and 2N HCl. The organic phase is washed with brine, dried over magnesium sulphate and concentrated to dryness. Recrystallization from ethyl acetate yields (E)-3-[4-(2,5-dimethyl-1-H-pyrrol-1-yl)-phenyl]-N-hydroxy-N-methyl-2-propenamide of Example 1.

후처리

  1. stirringThe mixture is stirred at room temperature for 30 minutes
  2. custompartitioned between ethyl acetate and 2N HCl
  3. washThe organic phase is washed with brine
  4. dry with materialdried over magnesium sulphate
  5. concentrationconcentrated to dryness
  6. customRecrystallization from ethyl acetate

출처 및 근거

ORD 기록
ord-631b651f058a404da581e2d5ff5b1a7c
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05096919

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