Sodium Carbonate → 4-Bromo-4'-(trifluoromethyl)biphenyl

HRID 1427507

反応式

HRID 1427507 の反応式
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:8]=[CH:7][C:6](B(O)O)=[CH:5][CH:4]=1.[Br:14][C:15]1[CH:20]=[CH:19][C:18](I)=[CH:17][CH:16]=1.C(=O)([O-])[O-].[Na+].[Na+]>CC([O-])=O.CC([O-])=O.[Pd+2]>[Br:14][C:15]1[CH:20]=[CH:19][C:18]([C:6]2[CH:7]=[CH:8][C:3]([C:2]([F:13])([F:12])[F:1])=[CH:4][CH:5]=2)=[CH:17][CH:16]=1

参加物

5

反応条件

温度
100 °C

実験手順

A 250 mL flask was charged with 4-(trifluoromethyl)phenylboronic acid (4.85 g, 25.5 mmol), 4-bromoiodobenzene (7.22 g, 25.5 mmol), Pd(OAc)2 (57.2 mg, 0.255 mmol) and sodium carbonate (5.41 g, 51.0 mmol). The flask was flushed with nitrogen, then n-propanol (40 mL) and water (8 mL) were added. The mixture was stirred at 100° C. overnight. The reaction mixture was cooled to room temperature and diluted with water. The mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The crude residue was purified by silica gel chromatography to provide 4-bromo-4′-(trifluoromethyl)biphenyl (5.4 g, 70%) as a colorless solid. 1H NMR (400 MHz, CDCl3) δ 7.62-7.73 (m, 4H), 7.57-7.61 (m, 2H), 7.43-7.47 (m, 2H).

後処理

  1. customThe flask was flushed with nitrogen
  2. additionn-propanol (40 mL) and water (8 mL) were added
  3. temperatureThe reaction mixture was cooled to room temperature
  4. additiondiluted with water
  5. extractionThe mixture was extracted with ethyl acetate
  6. washThe organic layer was washed with brine
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated under reduced pressure
  9. customThe crude residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-fb26d45eb4dd4d37b2a6d79b0db8319d
出典データセット
uspto-grants-2015_01
特許番号
US08933104B2

関連ノート

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