反応式
[C:1](Cl)(=[O:3])[CH3:2].C(N(CC)CC)C.[Br:12][C:13]1[CH:18]=[CH:17][C:16]([OH:19])=[C:15]([CH2:20][CH3:21])[CH:14]=1>C(Cl)Cl>[Br:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][C:1](=[O:3])[CH3:2])=[C:15]([CH2:20][CH3:21])[CH:14]=1参加物
5
実験手順
Acetyl chloride (1.06 mL, 14.9 mmol) followed by triethylamine (2.08 mL, 14.9 mmol) were added to a cooled 0° C. solution of 4-Bromo-2-ethyl-phenol (2.5 g, 12.4 mmol, from Step 1) dissolved in CH2Cl2. The reaction was stirred for 2 hrs and then partitioned between 1 N HCl and EtOAc. The organic layer was washed with saturated NaHCO3, brine, dried over Na2SO4 and concentrated to a brown oil. The oil was purified by silica gel chromatography (0% to 10% EtOAc in hexanes) to give the title compound as a clear oil (2.44 g, 81%).
後処理
- custompartitioned between 1 N HCl and EtOAc
- washThe organic layer was washed with saturated NaHCO3, brine
- dry with materialdried over Na2SO4
- concentrationconcentrated to a brown oil
- customThe oil was purified by silica gel chromatography (0% to 10% EtOAc in hexanes)
出典と根拠
- ORDレコード
- ord-c5e4098ac1994fd5aa5366136ac946ab
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- US07148226B2
関連ノート
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