反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[F:9].[H-].[Na+].[N+]([C:15]1[CH:16]=[C:17]([CH3:22])[N+:18]([O-:21])=[CH:19][CH:20]=1)([O-])=O>CN(C=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:15]2[CH:20]=[CH:19][N+:18]([O-:21])=[C:17]([CH3:22])[CH:16]=2)=[CH:4][C:3]=1[F:9]参加物
5
反応条件
- 温度
- 180 °C
実験手順
4-Bromo-3-fluorophenol (0.5 g, 2.61 mmol) was added to a solution of sodium hydride (0.115 g, 2.90 mmol) in DMF (5 ml). After stiffing for 10 minutes 4-nitro-2-picoline N-oxide (0.37 g, 2.41 mmol) was added. The reaction mixture was heated at 180° C. for 1 hour under microwave irradiation. After cooling to room temperature the mixture was filtered through diatomaceous earth and this was thoroughly washed with EtOAc. The filtrate was washed with water (2×25 ml), the organic fraction was dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 0-3% methanol/DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate D12 (0.33 g, 49%).
後処理
- temperatureAfter cooling to room temperature the mixture
- filtrationwas filtered through diatomaceous earth
- washthis was thoroughly washed with EtOAc
- washThe filtrate was washed with water (2×25 ml)
- dry with materialthe organic fraction was dried (Na2SO4)
- customthe solvent evaporated in vacuo
- customThe crude product was purified by column chromatography (silica gel; 0-3% methanol/DCM as eluent)
- customThe desired fractions were collected
- customevaporated in vacuo
- customto yield intermediate D12 (0.33 g, 49%)
出典と根拠
- ORDレコード
- ord-1dcfdd3f566349dbb75c98d9510b130b
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08748621B2
関連ノート
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