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Methyl iodide → 2-(Methylamino)-4-nitrophenol

HRID 1585098
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HRID 1585098 반응식
C([N:3]([CH2:6]C)[CH2:4][CH3:5])C.NC1C=[C:13]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:11][C:10]=1[OH:18].CI>CO>[CH3:6][NH:3][C:4]1[CH:5]=[C:13]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:11][C:10]=1[OH:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodide2회HCID 8471Triethylamine2회HCID 36133892-Amino-4-Nitrophenol

생성물 1

HCID 212217592-(Methylamino)-4-nitrophenol

시약·촉매·용매 1

HCID 887Methanol용매

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온도
40 °C

실험 절차

Triethylamine (2 ml, 14.4 mmol) was added to a solution of 2-amino-4-nitrophenol (1) (1.54 g, 10 mmol) and methyl iodide (1 ml, 16 mmol) in methanol (10 ml). After 1 hour at 40° C., further methyl iodide (1 ml) and triethylamine (1 ml) were added and the mixture was stirred at 40° C. for a further 2 hours. The reaction mixture was concentrated to dryness in vacuo, the residue was added to aqueous 2N sodium acetate solution and the mixture was extracted with ethyl acetate. The organic phase was dried with sodium sulfate and chromatographed on silica gel (eluent dichloromethane/methanol 95/5). Yield 880 mg (52%).

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후처리

  1. concentrationThe reaction mixture was concentrated to dryness in vacuo
  2. additionthe residue was added to aqueous 2N sodium acetate solution
  3. extractionthe mixture was extracted with ethyl acetate
  4. dry with materialThe organic phase was dried with sodium sulfate
  5. customchromatographed on silica gel (eluent dichloromethane/methanol 95/5)

출처 및 근거

ORD 기록
ord-66aae1aa20a84164b9801f127695ea82
출처 데이터셋
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05935995

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