Nitric Acid → 2-Bromo-3-methoxy-6-nitropyridine
反応式
S(=O)(=O)(O)O.[N+:6]([O-:9])(O)=[O:7].[Br:10][C:11]1[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[CH:13][N:12]=1>>[Br:10][C:11]1[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[C:13]([N+:6]([O-:9])=[O:7])[N:12]=1参加物
反応条件
- 温度
- 55 °C
実験手順
83 mL of conc. sulfuric acid was cooled down to −5° C., and 83 mL of 90% nitric acid was carefully added thereto. Subsequently, 20.69 g (corresponding to 110.04 mmol) of 2-bromo-3-methoxypyridine was carefully added thereto. After the reaction mixture was stirred in an ice bath for 5 minutes, the mixture was stirred at room temperature for 10 minutes, and then was heated to 55° C. and further stirred for an hour. After the reaction solution was cooled to room temperature, the reaction solution was poured little by little into crushed ice to generate precipitates. The precipitates were filtered and washed with water, and then dried over phosphorous pentoxide under reduced pressure, to obtain 17.41 g (corresponding to 74.71 mmol) of 2-bromo-3-methoxy-6-nitropyridine (FIG. 5, Step 2).
後処理
- stirringthe mixture was stirred at room temperature for 10 minutes
- stirringfurther stirred for an hour
- temperatureAfter the reaction solution was cooled to room temperature
- additionthe reaction solution was poured little by little
- custominto crushed ice
- customto generate precipitates
- filtrationThe precipitates were filtered
- washwashed with water
- dry with materialdried over phosphorous pentoxide under reduced pressure
出典と根拠
- ORDレコード
- ord-86a411f2ad02488a8c40f3eeb5b44cc1
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08022207B2
反応ノート
読み込み中…