Sodium Carbonate → 5-Bromo-2-fluoro-2',3'-dimethoxy-2''-fluoro-p-terphenyl
반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][C:11](B(O)O)=[C:10]([O:17][CH3:18])[C:9]=1[O:19][CH3:20].[F:21][C:22]1[CH:27]=[CH:26][C:25]([Br:28])=[CH:24][C:23]=1I.C(=O)([O-])[O-].[Na+].[Na+]>C1(C)C=CC=CC=1>[Br:28][C:25]1[CH:24]=[CH:23][C:22]([F:21])=[C:27]([C:11]2[CH:12]=[CH:13][C:8]([C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[F:1])=[C:9]([O:19][CH3:20])[C:10]=2[O:17][CH3:18])[CH:26]=1참가 물질
실험 절차
In the atmosphere of argon, 15.2 g of 2′-fluoro-2,3-dimethoxybiphenyl-4-boronic acid, 16.5 g of 2-fluoro-5-bromoiodobenzene, 1.27 g of tetrakistriphenylphosphine palladium (0), 180 mL of toluene and 90 mL of an aqueous 2M sodium carbonate solution were placed in a flask. The resulting solution was stirred with heating under reflux for 8 hours. After cooling to room temperature, the reaction solution was extracted with toluene. An aqueous phase was removed, and an organic phase was washed with saturated saline. The organic phase was dried with magnesium sulfate, and concentrated. Residues were purified by means of silica gel column chromatography, whereby 17.8 g (yield: 80%) of 5-bromo-2-fluoro-2′,3′-dimethoxy-2″-fluoro-p-terphenyl was obtained.
후처리
- temperaturewith heating
- temperatureunder reflux for 8 hours
- extractionthe reaction solution was extracted with toluene
- customAn aqueous phase was removed
- washan organic phase was washed with saturated saline
- dry with materialThe organic phase was dried with magnesium sulfate
- concentrationconcentrated
- customResidues were purified by means of silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-cef7121a837d4c3ebbcc09e0f5207a00
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08629430B2
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