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Pyridine → HCID 18921566, 화합물

HRID 1289428
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HRID 1289428 반응식
[F:1][C:2]([F:14])([F:13])[C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[CH:8][CH:7]=[CH:6]2.[Br:15]Br.N1C=CC=CC=1>ClC(Cl)(Cl)Cl>[Br:15][C:7]1[CH:8]=[N:9][C:10]2[C:5]([CH:6]=1)=[CH:4][C:3]([C:2]([F:1])([F:13])[F:14])=[CH:12][CH:11]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 24408BromineHCID 126475676-(Trifluoromethyl)quinoline

생성물 1

HCID 18921566HCID 18921566, 화합물

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매2회

실험 절차

19.7 g of 6-trifluoromethyl-quinoline is introduced into 200 ml of tetrachloromethane. 5.2 ml of bromine is instilled and the solution is refluxed for one hour. Within twenty minutes, 7.9 g of pyridine in 8 ml of tetrachloromethane is instilled in the boiling solution. After one hour, it is allowed to cool, decanted from the precipitated salt and the solution is concentrated by evaporation. After column chromatography, 14.6 g of 3-bromo-6-trifluoromethyl-quinoline of melting point 79° C. is obtained.

후처리

  1. temperaturethe solution is refluxed for one hour
  2. waitWithin twenty minutes
  3. temperatureto cool
  4. customdecanted from the precipitated salt
  5. concentrationthe solution is concentrated by evaporation

출처 및 근거

ORD 기록
ord-5dcd0cc6b6b646d4b45637753ec9eb4b
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05750526

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