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1,4-Dibromobenzene → 4'-Bromo[1,1'-biphenyl]-3-amine

HRID 253013
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HRID 253013 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][CH:3]=1.[NH2:9][C:10]1[CH:11]=[C:12](B(O)O)[CH:13]=[CH:14][CH:15]=1.C(=O)([O-])[O-].[Na+].[Na+].C(OCC)(=O)C>CN(C)C=O.O>[Br:8][C:5]1[CH:6]=[CH:7][C:2]([C:14]2[CH:13]=[CH:12][CH:11]=[C:10]([NH2:9])[CH:15]=2)=[CH:3][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 78041,4-DibromobenzeneHCID 8857Ethyl AcetateHCID 10340Sodium CarbonateHCID 922693-Aminophenylboronic acid

생성물 1

HCID 289112884'-Bromo[1,1'-biphenyl]-3-amine수율 57%

시약·촉매·용매 2

HCID 962Water용매2회
HCID 6228
Dimethylformamide
용매

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온도
80 °C

실험 절차

1,4-Dibromobenzene (311 mg, 1.3 mmol) and 201 mg (1.3 mmol) of 3-aminophenylboronic acid were dissolved in 17 ml of N,N-dimethylformamide and 4.2 ml of water. Tetrakistriphenylphosphine palladium (154 mg, 0.13 mmol) and 211 mg (2.0 mmol) of sodium carbonate were added to the solution, and the mixture was stirred at 80° C. for 3 hr. Ethyl acetate (60 ml) and 8.5 ml of water were added to the reaction solution, and the mixture was filtered through Celite. The organic layer as the filtrate was washed five times with 30 ml of water. The organic layer was dried over anhydrous sodium sulfate and was filtered. The solvent was then removed by distillation. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give 182 mg (yield 57%) of the title compound.

후처리

  1. filtrationthe mixture was filtered through Celite
  2. washThe organic layer as the filtrate was washed five times with 30 ml of water
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. filtrationwas filtered
  5. customThe solvent was then removed by distillation
  6. customThe residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1)

출처 및 근거

ORD 기록
ord-6edd673a2769430eb84b816708ba0fdf
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07871982B2

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