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Acetic Acid → HCID 22458230, 화합물

HRID 2368078
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HRID 2368078 반응식
[CH3:1][O:2][N:3]([CH3:14])[C:4](=[O:13])/[CH:5]=[CH:6]/[C:7]1[CH:12]=[CH:11][N:10]=[CH:9][CH:8]=1.[C:15]([OH:18])(=[O:17])C>CO.[Rh]>[CH3:1][O:2][N:3]([CH3:14])[C:4](=[O:13])[CH2:5][CH2:6][CH:7]1[CH2:8][CH2:9][N:10]([C:15]([O:18][C:7]([CH3:12])([CH3:8])[CH3:6])=[O:17])[CH2:11][CH2:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 57517481HCID 57517481, 화합물

생성물 1

HCID 22458230HCID 22458230, 화합물수율 165.7%

시약·촉매·용매 2

HCID 23948Rhodium촉매HCID 887Methanol용매

실험 절차

A solution of (2E)-N-methoxy-N-methyl-3-(pyridin-4-yl)prop-2-enamide (2.00 g), 5% rhodium/carbon (containing water (50%), 0.4 g) and acetic acid (1.25 g) in methanol (40 mL) was stirred for 4 hr under ice-cooling under a hydrogen atmosphere (5 atm). The reaction mixture was allowed to cool to room temperature and filtered, and the filtrate was concentrated under reduced pressure. The residue was dissolved in a mixed solvent of THF (25 mL) and water (10 mL), di-tert-butyl dicarbonate (4.36 g) and 2M aqueous sodium hydroxide solution (25 mL) were added, and the mixture was stirred at room temperature for 15 hr. The reaction mixture was diluted with ethyl acetate and water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (2.59 g).

후처리

  1. temperaturecooling under a hydrogen atmosphere (5 atm)
  2. filtrationfiltered
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. dissolutionThe residue was dissolved in a mixed solvent of THF (25 mL) and water (10 mL), di-tert-butyl dicarbonate (4.36 g) and 2M aqueous sodium hydroxide solution (25 mL)
  5. additionwere added
  6. additionThe reaction mixture was diluted with ethyl acetate and water
  7. extractionextracted with ethyl acetate
  8. washThe organic layer was washed with saturated brine
  9. dry with materialdried over anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure
  11. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-153291978b694f6e9bba1ac4b34554b4
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08703758B2

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