反応式
Br[C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[F:11])[C:5]([OH:7])=[O:6].[Li]CCCC.C([O:20][B:21](OC(C)C)[O:22]C(C)C)(C)C>C1COCC1.Cl>[OH:20][B:21]([OH:22])[C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[F:11])[C:5]([OH:7])=[O:6]参加物
6
反応条件
- 温度
- -78 °C
実験手順
To solution of 3-Bromo-4-fluoro-benzoic acid (1.0 eq) in THF (0.2M) at −78° C. was added n-BuLi (2.5M in Hex; 2.2 eq). The resulting mixture was stirred at −78° C. for 15 min then tri-isopropoxy borane (2.2 eq). The final mixture was stirred 1 h at −78° C. then 4 h at room temperature and finally poured in HCl (10%). After stirring for 12 h, THP was evaporated and the residual mixture was diluted with EtOAc. The organic extract was washed with HCl (10%), brine, dried over MgSO4, filtered and concentrated. The residue was suspended in EtOAc, stirred for 4 h and the desired compound was isolated by filtration.
後処理
- stirringAfter stirring for 12 h
- customTHP was evaporated
- additionthe residual mixture was diluted with EtOAc
- extractionThe organic extract
- washwas washed with HCl (10%), brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- stirringstirred for 4 h
出典と根拠
- ORDレコード
- ord-8c113f86f6b94efcb76b87754e5c89c9
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- US07144896B2
関連ノート
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