Borane → 3-Bromo-5-chlorophenol

HRID 1044702

反応式

HRID 1044702 の反応式
CP(C)CCP(C)C.[Br:9][C:10]1[CH:11]=[C:12]([Cl:16])[CH:13]=[CH:14][CH:15]=1.[B]1OC(C)(C)C(C)(C)[O:18]1.B.OOS([O-])=O.[K+]>CC(C)=O.O.C1CC=CCCC=C1.C1C=C[C]2[CH][CH][CH][C]2C=1.[Ir]>[Br:9][C:10]1[CH:15]=[C:14]([OH:18])[CH:13]=[C:12]([Cl:16])[CH:11]=1

参加物

9

反応条件

温度
150 °C

実験手順

Under an atmosphere of dry nitrogen, 103 mg 1,5-cyclooctadiene(H5-indenyl)iridium (I) was put in a 25 mL Pyrex bottle. Subsequently were added 0.04 mL 1,2-bis(dimethylphosphino)ethane, 0.61 mL 3-bromochlorobenzene and 1.52 mL pinacolborane. The mixture was stirred at 150° C. for 3.5 h. After cooling to room temperature, the borane adduct was taken up in 17 mL acetone to give a clear solution. This solution was added slowly to 17.41 mL of a 0.30 M solution of oxone in water cooled in an ice bath. The mixture was stirred vigorously for 15 min. at room temperature and extracted three times with DCM. The combined organic phases were dried over Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (DCM) to yield 750 mg (62%) of a beige solid. 1H NMR complies with known data (compound (I), Maleczka, 2003).

後処理

  1. temperatureAfter cooling to room temperature
  2. customto give a clear solution
  3. temperaturecooled in an ice bath
  4. stirringThe mixture was stirred vigorously for 15 min. at room temperature
  5. extractionextracted three times with DCM
  6. dry with materialThe combined organic phases were dried over Na2SO4
  7. customevaporated to dryness
  8. customThe residue was purified by flash chromatography (DCM)

出典と根拠

ORDレコード
ord-2b79712341fa47a1a049f74f73b13afe
出典データセット
uspto-grants-2013_10
特許番号
US08563723B2

関連ノート

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