(1,1'-Biphenyl)-2-ol → HCID 66845232, 화합물
반응식
[C:1]1(C2C=CC=CC=2O)C=CC=C[CH:2]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[C:20]([O:26][CH2:27][CH3:28])(=[O:25])[CH2:21][C:22]([O-:24])=[O:23].[Cl:29][C:30]1[CH:35]=[C:34]([F:36])[C:33](I)=[CH:32][C:31]=1[F:38].O1CCCC1>[NH4+].[Cl-].CCOC(C)=O.[Cu]I>[Cl:29][C:30]1[C:31]([F:38])=[CH:32][C:33]([CH:21]([C:22]([O:24][CH2:1][CH3:2])=[O:23])[C:20]([O:26][CH2:27][CH3:28])=[O:25])=[C:34]([F:36])[CH:35]=1참가 물질
반응물 5
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 90 °C
실험 절차
Copper(I) iodide (69.4 mg, 0.364 mmol), 2-phenylphenol (93.0 mg, 0.546 mmol) and cesium carbonate (1.78 g, 5.46 mmol) were added to a dry flask under nitrogen. Ethyl malonate (1.11 mL, 7.29 mmol) was added to the mixture, followed by 1-chloro-2,5-difluoro-4-iodobenzene (1.00 g, 3.64 mmol) in tetrahydrofuran (3.64 mL, 44.9 mmol). The reaction mixture was sealed and heated to 90° C. After 12 hours, the reaction mixture was allowed to cool to room temperature and then diluted with saturated NH4Cl and EtOAc. The organic layer was separated, dried and filtered through Celite. The brown oil was purified via silica gel chromatography (0-30% EtOAc-hexane) to give diethyl 2-(4-chloro-2,5-difluorophenyl)malonate (0.65 g, 58%). 1H NMR (400 MHz, CDCl3) δ 7.37 (dd, J=6.3, 9.3, 1H), 7.17 (dd, J=6.1, 8.9, 1H), 4.91 (s, 1H), 4.33-4.14 (m, 4H), 1.28 (t, J=7.2, 6H).
후처리
- customThe reaction mixture was sealed
- temperatureto cool to room temperature
- customThe organic layer was separated
- customdried
- filtrationfiltered through Celite
- customThe brown oil was purified via silica gel chromatography (0-30% EtOAc-hexane)
출처 및 근거
- ORD 기록
- ord-03a09f6221314ae6a2225c77d8c7daca
- 출처 데이터셋
- uspto-grants-2013_12
- 특허 번호
- US08618097B2
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