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4-Nitrophenol → Ethyl 4-nitrophenyl carbonate

HRID 1796191
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HRID 1796191 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1)([O-:3])=[O:2].Cl[C:12]([O:14][CH2:15][CH3:16])=[O:13].N1C=CC=CC=1.C(OCC)(=O)C>ClCCl>[C:12](=[O:13])([O:10][C:7]1[CH:8]=[CH:9][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=1)[O:14][CH2:15][CH3:16]
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참가 물질

6

반응물 4

HCID 9804-NitrophenolHCID 1049PyridineHCID 8857Ethyl AcetateHCID 10928Ethyl chloroformate

생성물 1

HCID 586863Ethyl 4-nitrophenyl carbonate수율 95%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 4-nitrophenol (1.00 g) in dichloromethane (20 ml) were added dropwise ethyl chloroformate (0.70 ml) and pyridine (0.70 ml) under ice-cooling, and the resulting mixture was stirred at room temperature overnight and then evaporated in vacuo. To the residue obtained was added ethyl acetate, and the organic layer was washed successively with a saturated aqueous sodium hydrogencarbonate solution, a saturated aqueous sodium chloride solution, a saturated aqueous potassium hydrogensulfate solution and a saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and evaporated in vacuo. The residual solid obtained was collected by filtration using hexane to afford ethyl 4-nitrophenyl carbonate (1.44 g, yield: 95%) as a white solid.

후처리

  1. temperaturecooling
  2. customevaporated in vacuo
  3. customTo the residue obtained
  4. washthe organic layer was washed successively with a saturated aqueous sodium hydrogencarbonate solution
  5. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  6. customevaporated in vacuo
  7. customThe residual solid obtained
  8. filtrationwas collected by filtration

출처 및 근거

ORD 기록
ord-1f796e95d6c7409b88e9c4087a261aa3
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07030138B2

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