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Acetic Acid → HCID 22458230、化合物

HRID 2368078
ノート
印刷プレビュー

反応式

HRID 2368078 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 176Acetic AcidHCID 57517481HCID 57517481、化合物

生成物 1

HCID 22458230HCID 22458230、化合物収率 165.7%

試薬・触媒・溶媒 2

HCID 23948Rhodium触媒HCID 887Methanol溶媒

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-153291978b694f6e9bba1ac4b34554b4
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08703758B2

反応ノート

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