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

HRID 2259565
ノート
印刷プレビュー

反応式

HRID 2259565 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 58012-AminophenolHCID 7923Maleic AnhydrideHCID 8471Triethylamine

生成物 1

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

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-c850ca0036c84f29b30fdcba2953b59f
出典データセット
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05474988

反応ノート

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