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Dimethylformamide → 9-Aminocarbazole

HRID 2051200
ノート
印刷プレビュー

反応式

HRID 2051200 の反応式
C[N:2](C)C=O.[CH:6]1[C:18]2[NH:17][C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10]=2[CH:9]=[CH:8][CH:7]=1.[OH-].[K+].NOS(O)(=O)=O>O>[CH:15]1[C:16]2[N:17]([NH2:2])[C:18]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[C:11]=2[CH:12]=[CH:13][CH:14]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6228DimethylformamideHCID 6854CarbazoleHCID 14797Potassium HydroxideHCID 76284hydroxylamine-O-sulfonic acid

生成物 1

HCID 2762079-Aminocarbazole

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Into 250 ml of dimethylformamide was dissolved 25 g of carbazole. This solution was cooled with an ice-salt bath and 42 g of potassium hydroxide was added portionwise. To this mixture was added hydroxylamine-O-sulfonic acid. After two hours the mixture was stirred with water and extracted with ethyl acetate. The organic extracts were washed with water and brine. After filtering the solvent was evaporated and the residue was eluted with 25% dichloromethane in hexane on a silica column to yield 9.5 g of a mixture of carbazole and 9H-carbazol-9-amine.

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

後処理

  1. temperatureThis solution was cooled with an ice-salt bath
  2. extractionextracted with ethyl acetate
  3. washThe organic extracts were washed with water and brine
  4. filtrationAfter filtering the solvent
  5. customwas evaporated
  6. washthe residue was eluted with 25% dichloromethane in hexane on a silica column

出典と根拠

ORDレコード
ord-5d62ab80ad564fa2a32f6ce73e22f750
出典データセット
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05017578

反応ノート

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