Hydrochloric Acid → 4-(Difluoromethoxy)benzeneboronic acid
반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH:9]([F:11])[F:10])=[CH:4][CH:3]=1.[B:12](OC(C)C)([O:17]C(C)C)[O:13]C(C)C.C([Li])CCC.Cl>O1CCCC1.O>[F:10][CH:9]([F:11])[O:8][C:5]1[CH:6]=[CH:7][C:2]([B:12]([OH:17])[OH:13])=[CH:3][CH:4]=1참가 물질
실험 절차
To a stirred solution of 1-bromo-4-(difluoromethoxy)-benzene (1.18 g) and triisopropyl borate (1.34 ml) in tetra-hydrofuran (6 ml) was added dropwise n-butyl lithium (1.58 M hexane solution, 3.68 ml) at −78° C. over 10 minutes under argon atmosphere, then the reaction mixture was allowed to warm to room temperature. After being starred at room temperature for 3 hours, the mixture was cooled to 0° C., and thereto were added a 6 N aqueous hydrochloric acid solution and water. The resultant mixture was extracted with ethyl acetate (30 ml) twice, and the combined organic layer was washed with brine (10 ml), dried over sodium sulfate. The insoluble materials were filtered off, and the filtrate was evaporated under reduced pressure. The residual solid was triturated with cold hexane to give the titled compound as a colorless solid. 1H-NMR (DMSO-d6) δ 7.12 (d, J=8.4 Hz, 2H), 7.27 (t, J=74.1 Hz, 1H), 7.83 (d, J=8.6 Hz, 2H), 8.08 (br-s, 2H).
후처리
- temperaturethe mixture was cooled to 0° C.
- extractionThe resultant mixture was extracted with ethyl acetate (30 ml) twice
- washthe combined organic layer was washed with brine (10 ml)
- dry with materialdried over sodium sulfate
- filtrationThe insoluble materials were filtered off
- customthe filtrate was evaporated under reduced pressure
- customThe residual solid was triturated with cold hexane
출처 및 근거
- ORD 기록
- ord-e4365e8441e044ae9e2c22b56690fbd2
- 출처 데이터셋
- uspto-grants-2011_05
- 특허 번호
- US07935674B2
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