Potassium Carbonate → Methyl 3-(cyanomethoxy)benzoate

HRID 1097463

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HRID 1097463 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].Br[CH2:13][C:14]#[N:15].C(=O)([O-])[O-].[K+].[K+].C(=O)([O-])O.[Na+]>CC(C)=O>[C:14]([CH2:13][O:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6])#[N:15]

참가 물질

6

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온도
60 °C

실험 절차

To a solution of methyl 3-hydroxybenzoate (5.00 g, 32.9 mmol) in acetone (60 mL) were added bromoacetonitrile (2.63 mL, 39.4 mmol) and potassium carbonate (6.81 g, 49.3 mmol), and the mixture was stirred at 60° C. for 4 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution (100 mL), and the mixture was extracted with ethyl acetate (100 mL, 30 mL). The combined organic layer was washed with saturated brine (10 mL), and dried over anhydrous magnesium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate/n-hexane=10/90→20/80), and the fraction containing the object product was concentrated under reduced pressure to give the title compound (5.43 g, 86%) as a colorless oil.

후처리

  1. extractionthe mixture was extracted with ethyl acetate (100 mL, 30 mL)
  2. washThe combined organic layer was washed with saturated brine (10 mL)
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationInsoluble material was filtered off
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe obtained residue was purified by basic silica gel column chromatography (ethyl acetate/n-hexane=10/90→20/80)
  7. additionthe fraction containing the object product
  8. concentrationwas concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-2510e4e7261945f0b7ad0f7a92b099fb
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08143258B2

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