反応 #969606
ord-86b105fd41c247008a6d61148fbbfc25
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1濃縮The reaction mixture was concentrated under reduced pressure
- 2その他then triturated with diethyl ether
- 3ろ過The suspension was filtered
- 4濃縮the filtrate was concentrated under reduced pressure
- 5その他Purification by flash chromatography (100% hexanes)
実験手順
Coupling of 3-bromophenol (17) (5.0 g, 28.9 mmol) with 2-ethylbutan-1-ol (3.25 g, 31.79 mmol) was conducted following the procedure given for Example 6. The reaction mixture was concentrated under reduced pressure then triturated with diethyl ether. The suspension was filtered and the filtrate was concentrated under reduced pressure. Purification by flash chromatography (100% hexanes) gave 1-bromo-3-(2-ethylbutoxy)benzene a clear liquid. Yield (5.04 g, 62%): 1H NMR (400 MHz, DMSO-d6) δ 7.20 (t, J=8.0 Hz, 1H), 7.11 (t, J=2.2 Hz, 1H), 7.07 (dd, J=8.0, 2.0 Hz, 1H), 6.92 (dd, J=8.4, 2.6 Hz, 1H), 3.84 (d, J=5.6 Hz, 2H), 1.61-1.53 (m, 1H), 1.46-1.30 (m, 4H), 0.86 (t, J=7.4 Hz, 6H).