반응 #2348084
ord-748b112e6ada4a7e9ddd25cdd65008f6
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반응 조건
후처리
- 1온도heated
- 2온도under reflux for 2 hours
- 3workup.ADDITIONmixed
- 4기타to be separated into two layers of an organic layer
- 5추출Extraction into an organic layer
- 6세척The extracts were washed with water
- 7건조dried over anhydrous magnesium sulfate
- 8농축The resulting solution was concentrated under reduced pressure
- 9기타the residue was purified by means
- 10기타of fraction-collecting column chromatography
- 11기타The solution was further purified by recrystallization from Solmix A-11
- 12기타dried
실험 절차
Into a reaction vessel under an atmosphere of nitrogen, 4-propyl phenylboronic acid (T16; 200.0 g), 1-bromo-3-fluorobenzene (T8; 177.8 g), potassium carbonate (281.9 g), Pd(Ph3P)2Cl2 (7.2 g), toluene (600 ml), and Solmix A-11 (600 ml) were put and heated under reflux for 2 hours. After the reaction mixture had been cooled to 25° C., the solution was poured into water (2,000 ml) and toluene (1,000 ml), and mixed. The mixture was then allowed to stand to be separated into two layers of an organic layer and an aqueous layer. Extraction into an organic layer was carried out and the resulting organic layer was fractionated. The extracts were washed with water, and dried over anhydrous magnesium sulfate. The resulting solution was concentrated under reduced pressure, and the residue was purified by means of fraction-collecting column chromatography using heptane as the eluent and silica gel as the stationary phase powder. The solution was further purified by recrystallization from Solmix A-11 and then dried, whereby 175.5 g of 3-fluoro-4′-propylbiphenyl (T17) was obtained. The yield based on the compound (T8) was 80.3%.