Methyl iodide → 2-Chloro-1-methoxy-3-methyl-4-nitrobenzene
反応式
[Cl:1][C:2]1[C:7]([CH3:8])=[C:6]([N+:9]([O-:11])=[O:10])[CH:5]=[CH:4][C:3]=1[OH:12].[H-].[Na+].[CH3:15]I>CN(C=O)C>[Cl:1][C:2]1[C:7]([CH3:8])=[C:6]([N+:9]([O-:11])=[O:10])[CH:5]=[CH:4][C:3]=1[O:12][CH3:15]参加物
5
実験手順
2-Chloro-3-methyl-4-nitrophenol (9.39 g, 50.0 mmol) was reacted with sodium hydride (50%, 2.64 g, 55.0 mmol) and methyl iodide (7.81 g, 55.0 mmol) in dry DMF (200 ml) by the method described in 1 (a). After treatment with water, the product was extracted with chloroform, and the dried extract evaporated to dryness, leaving an oil which crystallised on cooling, leaving solid 2-chloro-3-methyl-4-nitroanisole (8.19 g).
後処理
- extractionAfter treatment with water, the product was extracted with chloroform
- extractionthe dried extract
- customevaporated to dryness
- customleaving an oil which
- customcrystallised
- temperatureon cooling
出典と根拠
- ORDレコード
- ord-7a595a9bb28245488bfb0cabff633f57
- 出典データセット
- uspto-grants-1996_11
- 特許番号
- US05571833
反応ノート
読み込み中…