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2-Aminophenol → methyl 2-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)acetate

HRID 2259565
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반응식

HRID 2259565 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[C:9]1(=[O:15])[O:14][C:12](=[O:13])[CH:11]=[CH:10]1.[CH2:16](N(CC)CC)C>CO>[O:13]=[C:12]1[NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[O:8][CH:11]1[CH2:10][C:9]([O:14][CH3:16])=[O:15]
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참가 물질

5

반응물 3

HCID 58012-AminophenolHCID 7923Maleic AnhydrideHCID 8471Triethylamine

생성물 1

HCID 4428325methyl 2-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)acetate

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 76.4 g of 2-aminophenol and 68.6 g of maleic anhydride in 1 liter of methanol was stirred at room temperature. After addition of 100 ml of triethylamine, the yellow mass dissolved and the solution was heated for 7 hours at reflux temperature. The methanol was then removed by evaporation under reduced pressure, and the remaining oil was added to ice-water. The mixture was extracted with dichloromethane, and the organic extract was dried over sodium sulfate and evaporated. The remaining residue was crystallized from ethanol. In this way, 47.5 g of methyl (3-oxo-2,3-dihydro-4H-1,4-benzoxazin-2-yl)acetate were obtained as white crystals having a melting point of 140° C.

후처리

  1. dissolutionthe yellow mass dissolved
  2. temperaturethe solution was heated for 7 hours
  3. temperatureat reflux temperature
  4. customThe methanol was then removed by evaporation under reduced pressure
  5. additionthe remaining oil was added to ice-water
  6. extractionThe mixture was extracted with dichloromethane
  7. extractionthe organic extract
  8. dry with materialwas dried over sodium sulfate
  9. customevaporated
  10. customThe remaining residue was crystallized from ethanol

출처 및 근거

ORD 기록
ord-c850ca0036c84f29b30fdcba2953b59f
출처 데이터셋
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05474988

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