1-Bromo-2-Chloroethane → HCID 22326897、化合物
反応式
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[CH:6]=[CH:5][C:4]=1[OH:12].Br[CH2:14][CH2:15][Cl:16].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[Cl:16][CH2:15][CH2:14][O:12][C:4]1[CH:5]=[CH:6][C:7]([N+:9]([O-:11])=[O:10])=[CH:8][C:3]=1[O:2][CH3:1]参加物
5
反応条件
- 温度
- 90 °C
実験手順
A mixture of 2-methoxy-4-nitro-phenol (2.50 g, 14.8 mmol), 1-bromo-2-chloro-ethane (1.35 mL, 16.3 mmol) and potassium carbonate (4.08 g, 29.6 mmol) in DMF (50 mL) in a sealed tube was heated at 90° C. for 18 h. The reaction was cooled and filtered, washing with ethyl acetate. The filtrate was washed with sodium bicarbonate, water (4 times) and brine, was dried (sodium sulfate) and evaporated. Purification by flash chromatography (SiO2) eluted with 35:65 ethyl acetate:hexanes provided 1-(2-chloro-ethoxy)-2-methoxy-4-nitro-benzene (1.93 g, 56% yield) as an off-white solid. 1H-NMR (DMSO-d6, 500 MHz) 7.89 (dd, 1H), 7.76 (d, 1H), 7.21 (d, 1H), 4.41 (t, 2H), 4.00 (t, 2H), 3.90 (s, 3H) ppm; HPLC (Method A) 3.781 min.
後処理
- temperatureThe reaction was cooled
- filtrationfiltered
- washwashing with ethyl acetate
- washThe filtrate was washed with sodium bicarbonate, water (4 times) and brine
- dry with materialwas dried (sodium sulfate)
- customevaporated
- customPurification by flash chromatography (SiO2)
- washeluted with 35:65 ethyl acetate
出典と根拠
- ORDレコード
- ord-86fe6a3a92ec425d8b5f686d0b34f3d5
- 出典データセット
- uspto-grants-2011_03
- 特許番号
- US07902239B2
反応ノート
読み込み中…