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Methyl iodide → N-(3-Methoxy-4-nitrophenyl)acetamide

HRID 1773556
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HRID 1773556 반응식
[OH:1][C:2]1[CH:3]=[C:4]([NH:11][C:12](=[O:14])[CH3:13])[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9].[C:15](=O)([O-])[O-].[K+].[K+].CI.C(OCC)(=O)C>[Cl-].[Na+].O>[CH3:15][O:1][C:2]1[CH:3]=[C:4]([NH:11][C:12](=[O:14])[CH3:13])[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9]
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참가 물질

6

반응물 4

HCID 6328Methyl iodide2회HCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 10176525Acetamide, N-(3-hydroxy-4-nitrophenyl)-

생성물 1

HCID 13734467N-(3-Methoxy-4-nitrophenyl)acetamide

시약·촉매·용매 1

HCID 57417360Sodium chloride; water용매

실험 절차

To a solution of N-(3-hydroxy-4-nitro-phenyl)-acetamide (2 g, 10.15 mmol) in anhydrous N,N-dimethylormamide (5 mL) was added potassium carbonate (2.6 g, 18.88 mmol) followed by methyl iodide (0.71 mL, 11.16 mmol) and the reaction mixture was stirred at room temperature for 1 hour. A second aliquot of methyl iodide (0.15 mL) was then added and the resulting mixture was stirred for 1 hour. Ethyl acetate (100 mL) and brine (100 mL) were added, the organic layer was separated, washed twice with water, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to give N-(3-methoxy-4-nitro-phenyl)-acetamide.

후처리

  1. stirringthe resulting mixture was stirred for 1 hour
  2. customthe organic layer was separated
  3. washwashed twice with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-25166f50f9cb4497949ed93b617d5575
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09255110B2

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