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Ammonium formate → 1-[3-(Methoxycarbonyl)phenyl]nipecotic acid

HRID 602171
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HRID 602171 반응식
[CH:1]([O-:3])=[O:2].[NH4+:4].N1CCCC(C(OCC2([C:18]3[CH:23]=[CH:22][CH:21]=[C:20]([C:24]([O:26][CH3:27])=[O:25])[CH:19]=3)C=CC=CC2)=O)C1>[Pd].CO>[CH3:27][O:26][C:24]([C:20]1[CH:19]=[C:18]([N:4]2[CH2:22][CH2:23][CH2:18][CH:19]([C:1]([OH:3])=[O:2])[CH2:20]2)[CH:23]=[CH:22][CH:21]=1)=[O:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 866158861-[3-(Methoxycarbonyl)phenyl]benzyl nipecotate

생성물 1

HCID 589926191-[3-(Methoxycarbonyl)phenyl]nipecotic acid수율 180.7%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

In an argon atmosphere, 10% palladium on activated carbon (234 mg) and ammonium formate (1.66 g, 26.4 mmol) were added to 1-[3-(methoxycarbonyl)phenyl]benzyl nipecotate (2.34 g, 6.60 mmol) in methanol (50 mL). The reaction mixture was stirred at room temperature for 4 hours. Subsequently, the mixture was filtered through Celite and the filtrate was concentrated. 5% aqueous citric acid was added to the residue and the mixture was extracted with ethyl acetate. The organic layer was then washed with brine and was dried over sodium sulfate. The solvent was evaporated to give 1.57 g (90%) of the desired compound as a pale reddish brown powder.

후처리

  1. filtrationSubsequently, the mixture was filtered through Celite
  2. concentrationthe filtrate was concentrated
  3. addition5% aqueous citric acid was added to the residue
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe organic layer was then washed with brine
  6. dry with materialwas dried over sodium sulfate
  7. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-63aedc74330e42e6bd361332d1b1bf94
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07902367B2

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