반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][O:9][CH2:10][CH2:11][CH2:12][CH3:13])=[CH:4][CH:3]=1.C([Li])CCC.CN(C)[CH:21]=[O:22]>O1CCCC1>[CH2:10]([O:9][CH2:8][C:5]1[CH:6]=[CH:7][C:2]([CH:21]=[O:22])=[CH:3][CH:4]=1)[CH2:11][CH2:12][CH3:13]참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
To a solution of 1-bromo-4-butoxymethyl-benzene (11.5 g, 47.3 mmol) described in Manufacturing Example 4-1-1 in tetrahydrofuran (200 mL) was added n-butyl lithium (32.5 mL, 1.6 M hexane solution, 52.0 mmol) at −78° C. This mixture was stirred for 55 minutes at −78° C., and N,N-dimethylformamide (4.4 mL, 56.8 mmol) was added thereto at −78° C. This mixture was warmed to room temperature, and stirred for 20 minutes. The reaction solution was partitioned into water and ethyl acetate at 0° C. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1) to obtain the title compound (7.39 g, 81%).
후처리
- customat −78° C
- temperatureThis mixture was warmed to room temperature
- stirringstirred for 20 minutes
- customThe reaction solution was partitioned into water and ethyl acetate at 0° C
- washThe organic layer was washed with saturated aqueous sodium chloride
- dry with materialdried over anhydrous magnesium sulfate
- customthe solvent was evaporated under a reduced pressure
- customThe residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1)
출처 및 근거
- ORD 기록
- ord-b063cf59261d42cb82348c2133f3d949
- 출처 데이터셋
- uspto-grants-2010_04
- 특허 번호
- US07691882B2
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