Triisopropyl borate → 2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)
反応式
C([Li])CCC.Br[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:13][C:14]([F:17])([F:16])[F:15].[B:18](OC(C)C)([O:23]C(C)C)[O:19]C(C)C>O1CCCC1>[F:15][C:14]([F:17])([F:16])[O:13][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[B:18]([OH:23])[OH:19]参加物
5
実験手順
n-Butyllithium (5.9 ml, 9.5 mmol) was added to a solution of 1-bromo-2-(trifluoromethoxy)benzene (2 g, 8.2 mmol) in tetrahydrofuran (28 ml) at −78° C. and stirred for 45 minutes. Triisopropyl borate (2.58 ml, 11.1 mmol) was added dropwise to the reaction mixture and the solution was slowly brought to room temperature over 16 hours. The reaction mixture was quenched with water, made basic with 2N NaOH and extracted with ethyl acetate. The aqueous solution was acidified with 2N HCl, stirred for 1 hour at room temperature and extracted into ethyl acetate. The organic layer was washed with water, brine solution and dried over sodium sulfate. It was filtered and concentrated to give the product (1.10 g, 65%) as a white solid.
後処理
- waitthe solution was slowly brought to room temperature over 16 hours
- customThe reaction mixture was quenched with water
- extractionextracted with ethyl acetate
- stirringstirred for 1 hour at room temperature
- extractionextracted into ethyl acetate
- washThe organic layer was washed with water, brine solution
- dry with materialdried over sodium sulfate
- filtrationIt was filtered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-41a0f08520bb40a6aeb54dd67026c9ca
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07589116B2
反応ノート
読み込み中…