Potassium Carbonate → (E)-ethyl 2-(4-(methoxymethoxy)phenyl)-3-o-tolylpent-2-enoate
反応式
[C:1]([O:7][CH2:8][CH3:9])(=[O:6])[C:2]#[C:3][CH2:4][CH3:5].I[C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][O:19][CH3:20])=[CH:13][CH:12]=1.[CH3:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1B(O)O.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C.C1C=CC(C#N)=CC=1.C1C=CC(C#N)=CC=1.Cl[Pd]Cl.O>[CH3:20][O:19][CH2:18][O:17][C:14]1[CH:15]=[CH:16][C:11](/[C:2](=[C:3](\[C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=2[CH3:21])/[CH2:4][CH3:5])/[C:1]([O:7][CH2:8][CH3:9])=[O:6])=[CH:12][CH:13]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
A mixture of Ethyl 2-pentynoate (350 mg, 2.77 mmol), 1-iodo-4-(methoxymethoxy)benzene (1.46 g, 5.53 mmol), 2-Methylphenylboronic acid (753 mg, 5.53 mmol) and K2CO3 (766 mg, 5.54 mmol) in DMF (8.5 ml)-H2O (2.2 ml) was stirred at room temperature for 10 min. Then PdCl2(PhCN)2 (10.6 mg, 0.0276 mmol) was added under Ar atmosphere, and the mixture was stirred at room temperature for 24 h. The reaction was quenched with H2O under ice cooling, and the whole was extracted with Et2O. The organic layer was washed with H2O, brine, dried over Na2SO4, then concentrated. Purification by silica gel flash column chromatography (eluent: hexane/AcOEt, 30:1) gave 2a (27%). 2a: colorless oil; 1H-NMR (CDCl3) δ 1.02 (3H, t, J=7.5 Hz), 1.33 (3H, t, J=7.1 Hz), 2.04 (3H, s), 2.56 (2H, m), 3.42 (3H, s), 4.30 (2H, m), 5.06 (2H, s), 6.72 (2H, d, J=8.8 Hz), 6.88 (2H, d, J=8.8 Hz), 7.00-7.12 (5H, m).
後処理
- stirringthe mixture was stirred at room temperature for 24 h
- customThe reaction was quenched with H2O under ice cooling
- extractionthe whole was extracted with Et2O
- washThe organic layer was washed with H2O, brine
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customPurification by silica gel flash column chromatography (eluent: hexane/AcOEt, 30:1)
出典と根拠
- ORDレコード
- ord-73d9815309334c659f434151f4e29d34
- 出典データセット
- uspto-grants-2012_08
- 特許番号
- US08236987B2
反応ノート
読み込み中…