Sodium Carbonate → 5-Bromo-2-fluoro-2',3'-dimethoxy-2''-fluoro-p-terphenyl
反応式
[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]=1参加物
実験手順
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.
後処理
- 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
出典と根拠
- ORDレコード
- ord-e6c1dcb6bb3f455d9017790490222468
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08866135B2
反応ノート
読み込み中…