Nitric Acid → 2-Bromo-3-methoxy-6-nitropyridine
反応式
[Br:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[N+:10]([O-])([OH:12])=[O:11]>S(=O)(=O)(O)O>[Br:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][CH:5]=[C:4]([N+:10]([O-:12])=[O:11])[N:3]=1参加物
反応条件
- 温度
- 60 °C
実験手順
To a 500 mL round bottomed flask fitted with a Teflon stir bar and a thermometer was added 90 mL of concentrated sulphuric acid and 37.6 g of 2-bromo-3-methoxypyridine (200 mmol). The flask was warmed in an oil bath to 60° C. Added slowly over 1h 16.5 mL (350 mmol) of fuming nitric acid (90%, d=1.50). Maintain the temperature between 60 and 70° during the addition. Stir at 60° for 3h after the addition was complete, then at room temperature overnight. By TLC (70/30 hex/EtOAc) is consumed. The product mixture was poured into 600 mL of ice/water, from which the product precipitated. This material was filtered, washed with 3×200 mL of cold water and then 100 mL of saturated sodium bicarbonate. After drying in the filter funnel in a stream of air, the remaining water was removed under reduced pressure, to give 16.5 g of a solid. H NMR (400 MHz, CDCl3): δ 8.27(d, J=8 Hz,1H); 6.32(d, J=8 Hz,1H); 4.06(s, 3H).
後処理
- temperatureMaintain the temperature between 60 and 70°
- additionduring the addition
- additionafter the addition
- customat room temperature
- customovernight
- customBy TLC (70/30 hex/EtOAc) is consumed
- additionThe product mixture was poured into 600 mL of ice/water, from which the product
- customprecipitated
- filtrationThis material was filtered
- washwashed with 3×200 mL of cold water
- customAfter drying in the filter funnel in a stream of air
- customthe remaining water was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-498afe0170b9453ab3a7132d2fbfce6c
- 出典データセット
- uspto-grants-1999_07
- 特許番号
- US05929094
反応ノート
読み込み中…