Hexane → HCID 69203973、化合物
反応式
Br[C:2]1[CH:12]=[CH:11][C:5]2[O:6][CH2:7][CH2:8][CH2:9][O:10][C:4]=2[CH:3]=1.C([Li])CCC.CCCCCC.[CH3:24][O:25][C:26]1[CH:27]=[C:28]([CH:31]=[C:32]([O:34][CH3:35])[CH:33]=1)[CH:29]=[O:30]>C1COCC1.O.C(O)(C)C>[O:6]1[CH2:7][CH2:8][CH2:9][O:10][C:4]2[CH:3]=[C:2]([CH:29]([C:28]3[CH:31]=[C:32]([O:34][CH3:35])[CH:33]=[C:26]([O:25][CH3:24])[CH:27]=3)[OH:30])[CH:12]=[CH:11][C:5]1=2参加物
実験手順
To a solution of 7-bromo-3,4-dihydro-2H-benzo[b][1,4]dioxepine (1.7 g, 7.4 mmol) in THF (10 mL) was added a solution of n-butyllitium in hexane (2.6 mL, 2.5 N, 6.5 mmol) at −78° C. and kept for 20 min. To the mixture was added a solution of 3,5-dimethoxy-benzaldehyde (1.0 g, 6.0 mmol) in THF (10 mL) at −78° C. After 2 h, isopropanol (2 mL) and water (10 mL) was added to the mixture, and the cold bath was removed. The mixture was stirred at room temperature for 20 min. The mixture was extracted with ethyl acetate (50 mL) and water (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL). The combined organic layers was washed with HCl (1N, 50 mL), water (50 mL), brine (50 mL) and dried over MgSO4. Removal of solvent and chromatography (Silica Gel) gave (3,4-dihydro-2H-benzo[b][1,4]dioxepin-7-yl)-(3,5-dimethoxy-phenyl) -methanol as an oil (1.8 g, 95% yield): 1H NMR (CDCl3) δ 2.16-2.22 (m, 2H, CH2), 3.77 (s, 6H, 2CH3), 4.16-4.21 (m, 4H, 2CH2), 5.67 (d, J=3 Hz, 1H, CH), 6.35 (t, J=2 Hz, 1H, Ar), 6.54 (d, J=2 Hz, 1H, Ar), 6.92 (d, J=1 Hz, 2H, Ar), 6.98 (s, 1H, Ar).
後処理
- waitAfter 2 h
- customthe cold bath was removed
- extractionThe mixture was extracted with ethyl acetate (50 mL) and water (50 mL)
- extractionThe aqueous layer was extracted with ethyl acetate (50 mL)
- washThe combined organic layers was washed with HCl (1N, 50 mL), water (50 mL), brine (50 mL)
- dry with materialdried over MgSO4
- customRemoval of solvent and chromatography (Silica Gel)
出典と根拠
- ORDレコード
- ord-848b6754f118489898ada89e610b9894
- 出典データセット
- uspto-grants-2008_12
- 特許番号
- US07470723B2
反応ノート
読み込み中…