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Sodium Carbonate → Ethanone, 1-(2-aminophenyl)-, oxime

HRID 580452
ノート
印刷プレビュー

反応式

HRID 580452 の反応式
[C:1]([C:4]1[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=1[NH2:6])(=O)[CH3:2].Cl.[NH2:12][OH:13].C(=O)([O-])[O-].[Na+].[Na+]>C(O)C>[C:1](=[N:12][OH:13])([C:4]1[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=1[NH2:6])[CH3:2]
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 10340Sodium CarbonateHCID 110862'-Aminoacetophenone2 回HCID 443297Hydroxyamine hydrochloride

生成物 1

HCID 2797858Ethanone, 1-(2-aminophenyl)-, oxime

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

2-Acetylaniline, 33.8 gm, was added slowly to 300 ml of ethanol containing 18.3 gm of hydroxylamine hydrochloride and 27.7 gm sodium carbonate. After addition of the entire amount of 2-acetylaniline, the system was refluxed for 16 hours and then cooled to room temperature. After cooling, the ethanol was removed by stripping. Water was then added to the residue to give a precipitate. The precipitate was filtered and dried to give a pale yellow solid, m.p. 55°-60° C.

後処理

  1. temperaturethe system was refluxed for 16 hours
  2. temperatureAfter cooling
  3. customthe ethanol was removed by stripping
  4. additionWater was then added to the residue
  5. customto give a precipitate
  6. filtrationThe precipitate was filtered
  7. customdried
  8. customto give a pale yellow solid, m.p. 55°-60° C.

出典と根拠

ORDレコード
ord-7936fbd2671a4dbeac68af9d367419b3
出典データセット
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04753943

反応ノート

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