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
反応物 5
生成物 1
試薬・触媒・溶媒 3
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 (1), Maleczka, 2003).
後処理
- temperatureAfter cooling to room temperature
- customto give a clear solution
- temperaturecooled in an ice bath
- stirringThe mixture was stirred vigorously for 15 min. at room temperature
- extractionextracted three times with DCM
- dry with materialThe combined organic phases were dried over Na2SO4
- customevaporated to dryness
- customThe residue was purified by flash chromatography (DCM)
出典と根拠
- ORDレコード
- ord-a5a2626f91834e989eac6b6c555d3aa3
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09126942B2
関連ノート
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