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Sodium Carbonate → 4-(2-Methoxy-5-nitrophenyl)pyridine

HRID 1358944
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HRID 1358944 반응식
Br[C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[O:11][CH3:12].[N:13]1[CH:18]=[CH:17][C:16](B(O)O)=[CH:15][CH:14]=1.C(=O)([O-])[O-].[Na+].[Na+]>COCCOC>[CH3:12][O:11][C:3]1[CH:4]=[CH:5][C:6]([N+:8]([O-:10])=[O:9])=[CH:7][C:2]=1[C:16]1[CH:17]=[CH:18][N:13]=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10340Sodium CarbonateHCID 788702-Bromo-4-nitroanisoleHCID 2734379(Pyridin-4-yl)boronic acid

생성물 1

HCID 144519694-(2-Methoxy-5-nitrophenyl)pyridine

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

A stirred mixture of 2-bromo-4-nitroanisole (7.6 g, 32.7 mmol), 4-pyridineboronic acid (4.07 g, 33 mmol) and powdered sodium carbonate (13.8 g, 5 equivalents) in 1:1 1,2-dimethoxyethane:water (1,360 ml) was degassed for 0.5 hr, by the passage of a stream of argon. Tetrakistriphenylphosphine palladium (0) (1.35 g) was added, and the mixture was cooled, the solvents evaporated under reduced pressure to approximately half-volume, and the aqueous residue was acidified with 5N hydrochloric acid and washed with ethyl acetate. The acid phase was then basified with solid potassium carbonate, and extracted into ethyl acetate, the organic phase was dried (Na2SO4) and evaporated under reduced pressure to give the title compound (D36) as a pale yellow solid (3.4 g, 45%).

후처리

  1. customwater (1,360 ml) was degassed for 0.5 hr, by the passage of a stream of argon
  2. additionTetrakistriphenylphosphine palladium (0) (1.35 g) was added
  3. temperaturethe mixture was cooled
  4. customthe solvents evaporated under reduced pressure to approximately half-volume
  5. washwashed with ethyl acetate
  6. extractionextracted into ethyl acetate
  7. dry with materialthe organic phase was dried (Na2SO4)
  8. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-e98fcf6d94e7492c983a954f23aeb359
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06599904B2

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