反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([S:8][CH3:9])=[CH:4][CH:3]=1.[Li][C:11](C)(C)C.[CH3:15][O:16][C:17](=[O:29])[C:18]1[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][C:19]=1Br>O1CCCC1.[Cl-].[Cl-].[Zn+2].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[Cl-].[Cl-].[Ni+2]>[CH3:11][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH3:9])=[CH:4][C:3]=1[C:19]1[CH:20]=[C:21]([C:22]([O:24][CH3:25])=[O:23])[CH:26]=[CH:27][C:18]=1[C:17]([O:16][CH3:15])=[O:29]参加物
実験手順
4-Bromothioanisole (7.1 g) was dissolved in tetrahydrofuran (23 ml). To this solution at -78° C. under nitrogen was added over a ten minute period 1.7M tBuLi (48 ml). After 45 minutes at room temperature, 1M ZnCl2 (41 ml) was added dropwise over a ten minute period. After one half hour at room temperature, bis(triphenylphosphine)nickel (II) chloride (1.4 g) was added followed by dimethyl-2-bromoterepthalate (4.67 g) in tetrahydrofuran (47 ml). The reaction mixture was stirred at room temperature for 45 minutes. The THF was removed under reduced pressure. The residue was treated with ethyl acetate and 1N HCl and the layers separated. The organic phase was washed with water, brine, dried over magnesium sulfate and evaporated gave the crude product. Chromatography on silica gel using 15% ethyl acetate/hexanes gave the desired product (3.92 g).
後処理
- waitAfter one half hour at room temperature
- customThe THF was removed under reduced pressure
- additionThe residue was treated with ethyl acetate and 1N HCl
- customthe layers separated
- washThe organic phase was washed with water, brine
- dry with materialdried over magnesium sulfate
- customevaporated
- customgave the crude product
出典と根拠
- ORDレコード
- ord-7b007aac96c4449dbda050f0741bda68
- 出典データセット
- uspto-grants-1992_09
- 特許番号
- US05144028
関連ノート
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