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10-Methoxyiminostilbene → DE(5-carboxamide)oxcarbazepine

HRID 2393731
ノート
印刷プレビュー

反応式

HRID 2393731 の反応式
C[O:2][C:3]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[NH:7][C:6]2[CH:14]=[CH:15][CH:16]=[CH:17][C:5]=2[CH:4]=1>Cl>[O:2]=[C:3]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[NH:7][C:6]2[CH:14]=[CH:15][CH:16]=[CH:17][C:5]=2[CH2:4]1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 7842410-Methoxyiminostilbene

生成物 1

HCID 11160106DE(5-carboxamide)oxcarbazepine

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

22.3 g of 10-methoxy-5H-dibenz(b,f)azepine are heated under reflux with 100 ml of 2N hydrochloric acid for 2 hours. The gummy residue is extracted with chloroform (50÷50 ml), the combined extracts are washed with water and evaporated to dryness under vacuum. The residue is taken up into 200 ml of ethanol, treated with charcoal (2 g) for 1 h under reflux, filtered, evaporated to dryness under vacuum, finally taken up into 50÷50 ml of toluene, stripping thoroughly. The residue is kept for further working-up.

後処理

  1. extractionThe gummy residue is extracted with chloroform (50÷50 ml)
  2. washthe combined extracts are washed with water
  3. customevaporated to dryness under vacuum
  4. additiontreated with charcoal (2 g) for 1 h
  5. temperatureunder reflux
  6. filtrationfiltered
  7. customevaporated to dryness under vacuum

出典と根拠

ORDレコード
ord-9f518891f9d3470ca3e74e568cdebc92
出典データセット
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05808058

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート