Potassium Iodide → Methyl 6-bromo-3-[(2-ethoxycarbonyl)propan-2-yl]amino-2-nitrobenzoate
反応式
[NH2:1][C:2]1[C:3]([N+:13]([O-:15])=[O:14])=[C:4]([C:9]([Br:12])=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].Br[C:17]([CH3:24])(C)[C:18]([O:20][CH2:21][CH3:22])=[O:19].[I-].[K+].[C:27](=O)([O-])[O-].[Cs+].[Cs+]>O.C(OCC)(=O)C>[Br:12][C:9]1[C:4]([C:5]([O:7][CH3:8])=[O:6])=[C:3]([N+:13]([O-:15])=[O:14])[C:2]([NH:1][CH:24]([CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])[CH3:27])=[CH:11][CH:10]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
The mixture of methyl 3-amino-6-bromo-2-nitrobenzoate (Reference Compound No. 1-(4), 11.6 g, 42.0 mmol), ethyl 2-bromoisobutyrate (60.4 mL, 412 mmol), potassium iodide (7.76 g, 46.2 mmol) and cesium carbonate (56.1 g, 172 mmol) was stirred at 85° C. for 4 days. After the mixture was cooled down, ethyl acetate (500 mL) and water (500 mL) were added thereto, the mixture was partitioned, and then the water layer was extracted with ethyl acetate (300 mL). The organic layer was combined, washed with water (1 L, 2 times) and saturated brine (1 L) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (5.08 g) as an orange oil. (Yield 31%)
後処理
- temperatureAfter the mixture was cooled down
- customthe mixture was partitioned
- extractionthe water layer was extracted with ethyl acetate (300 mL)
- washwashed with water (1 L, 2 times) and saturated brine (1 L) successively
- dry with materialdried over anhydrous magnesium sulfate
- customthe solvent was removed under reduced pressure
- customThe obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate)
出典と根拠
- ORDレコード
- ord-5fa380c36c3841538b1a1e43f565ed85
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08975256B2
反応ノート
読み込み中…