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Dimethylformamide → 9-Aminocarbazole

HRID 703468
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HRID 703468 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

HCID 2762079-Aminocarbazole

시약·촉매·용매 1

HCID 962Water용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-59196a714c484b80bb323ba5d61c2232
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04983608

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