Sodium Carbonate → 2-(3-Methoxyphenyl)-6,7-dihydro-5H-benzo[b]thiophen-4-one
反応式
Br[C:2]1[S:6][C:5]2[CH2:7][CH2:8][CH2:9][C:10](=[O:11])[C:4]=2[CH:3]=1.B(O)O.[CH3:15][O:16][C:17]1[CH:18]=[C:19](O)[CH:20]=[CH:21][CH:22]=1.C([O-])([O-])=O.[Na+].[Na+].CCO.O>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.COCCOC>[CH3:15][O:16][C:17]1[CH:22]=[C:21]([C:2]2[S:6][C:5]3[CH2:7][CH2:8][CH2:9][C:10](=[O:11])[C:4]=3[CH:3]=2)[CH:20]=[CH:19][CH:18]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
To 2-bromo-6,7-dihydro-5H-benzo[b]thiophen-4-one (5 g, 21.74 mmol) was successively added 3-methoxyphenol boronic acid (3.63 g, 23.92 mmol), 2M Na2CO3(aq) (43.5 mL, 86.98 mmol), Pd(PPh3)4 (251mg, 0.22 mmol), 3:4 EtOH/H2O (37.5 mL) and DME (62.5 mL). The reaction mixture was degassed and heated to reflux for 12 hours. EtOAc (250 mL) was added and the crude reaction mixture was washed with water (2×100 mL). The organic layer was dried over magnesium sulphate, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with EtOAc:hexanes (20:80) to give the title compound as an off-white solid in 95% yield. MS (ES+) 259. δH (d6 DMSO) 2.13 (2H, quint.), 2.50 (2H, m), 3.05 (2H, t), 3.81 (3H, s), 6.91 (1H, m), 7.20-7.22 (2H, m), 7.34 (1H, m), 7.67 (1H, s).
後処理
- customThe reaction mixture was degassed
- temperatureheated
- temperatureto reflux for 12 hours
- additionEtOAc (250 mL) was added
- customthe crude reaction mixture
- washwas washed with water (2×100 mL)
- dry with materialThe organic layer was dried over magnesium sulphate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified by silica gel chromatography
- washeluting with EtOAc:hexanes (20:80)
出典と根拠
- ORDレコード
- ord-55a137c968b5499b8ef3005f8b13e7ae
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07700609B2
反応ノート
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