5-Bromo-2,3-dichlorotoluene → HCID 66865196、化合物
反応式
[Br-].[F:2][C:3]([F:8])([F:7])[C:4]([Zn+])=[CH2:5].Br[C:10]1[CH:11]=[C:12]([Cl:18])[C:13]([Cl:17])=[C:14]([CH3:16])[CH:15]=1>O1CCCC1.CN(C)C=O>[Cl:18][C:12]1[CH:11]=[C:10]([C:4]([C:3]([F:8])([F:7])[F:2])=[CH2:5])[CH:15]=[C:14]([CH3:16])[C:13]=1[Cl:17]参加物
反応条件
- 温度
- 100 °C
実験手順
To 1M solution of 1-(trifluoromethyl)ethenyl zinc bromide in tetrahydrofuran (see J. Org. Chem. 1991, 56, 7336 for preparation) (19 mL) was added a solution of 5-bromo-2,3-dichlorotoluene (2.2 g) in N,N-dimethylformamide (10 mL), then tetrahydrofuran was distilled off under reduced pressure. Dichlorobis(triphenylphosphine)palladium(II) (0.26 g) was added to the residual N,N-dimethylformamide solution, which was stirred at 100° C. for 3.5 hours under nitrogen atmosphere and then cooled to room temperature. To the resulting mixture was added tetrahydrofuran-hexane 2:5 mixture (200 mL) and filtered, and the filtrate was washed with water (100 mL) and brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide a residue. The residue was purified by column chromatography on silica gel eluted with hexane to afford the title compound as a brown oil (2.3 g).
後処理
- distillationtetrahydrofuran was distilled off under reduced pressure
- additionDichlorobis(triphenylphosphine)palladium(II) (0.26 g) was added to the residual N,N-dimethylformamide solution, which
- temperaturecooled to room temperature
- additionTo the resulting mixture was added tetrahydrofuran-hexane 2:5 mixture (200 mL)
- filtrationfiltered
- washthe filtrate was washed with water (100 mL) and brine
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated under reduced pressure
- customto provide a residue
- customThe residue was purified by column chromatography on silica gel
- washeluted with hexane
出典と根拠
- ORDレコード
- ord-bc0bd53f42674413aa1656d6e7b94e30
- 出典データセット
- uspto-grants-2012_08
- 特許番号
- US08242283B2
反応ノート
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