反応式
[CH3:1][O:2][C:3]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:4]=1[OH:5]>O>[CH3:1][O:2][C:3]1[C:4](=[O:5])[CH:6]=[CH:7][C:8](=[O:10])[CH:9]=1参加物
3
実験手順
In a 500 mL beaker NaIO4 (Baker, used as received, 10.6 g, 49.6 mmol) was dissolved in water (distilled, 450 mL) and stirred magnetically. 2-Methoxyhydroquinone (2.2 g, 15.7 mmol) was added giving an orange solution. The mixture was stirred at rt for 1 h then extracted with CH2Cl2 (3×100 mL). The organic extract was washed with brine (1×100 mL), dried by filtering through cotton and evaporated to dryness (roto-vap) giving 2-methoxy-1,4-benzoquinone as a yellow solid (2.1 g, 97%, one spot on TLC, Rf =0.5, >95% pure by 1H NMR): mp 141°-143° C., 1H NMR (CDCl3) δ3.85 (s, 3H), 5.98 (s, 1H), 6.75 (s, 2H).
後処理
- customgiving an orange solution
- stirringThe mixture was stirred at rt for 1 h
- extractionthen extracted with CH2Cl2 (3×100 mL)
- extractionThe organic extract
- washwas washed with brine (1×100 mL)
- customdried
- filtrationby filtering through cotton
- customevaporated to dryness (roto-vap)
出典と根拠
- ORDレコード
- ord-782dbde2d0e74259a7abeb0fab8a7583
- 出典データセット
- uspto-grants-1998_01
- 特許番号
- US05708168
関連ノート
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