反応式
[NH2:1][C:2]1[CH:7]=[N:6][C:5]([CH3:8])=[CH:4][N:3]=1.O.O.O.C([O-])(=O)C.[Na+].[Br:17]Br.[OH-].[Na+]>C(O)(=O)C>[NH2:1][C:2]1[C:7]([Br:17])=[N:6][C:5]([CH3:8])=[CH:4][N:3]=1参加物
6
反応条件
- 温度
- 20 °C
実験手順
To acetic acid (1500 ml.), 2-amino-5-methylpyrazine (1 mole) and 326.5 g. sodium acetate trihydrate are slowly added 1.1 mole bromine in 180 ml. acetic acid at 2° C. in the absence of light. The mixture is stirred about 15 hours at 20° C., stripped of acetic acid in vacuo, poured into ice, made alkaline with sodium hydroxide, filtered, the residue extracted with ether, the extract stripped and the 2-amino-3-bromo-5-methylpyrazine crystallized from a suitable solvent.
後処理
- customat 2° C.
- additionpoured into ice
- filtrationfiltered
- extractionthe residue extracted with ether
- customthe 2-amino-3-bromo-5-methylpyrazine crystallized from a suitable solvent
出典と根拠
- ORDレコード
- ord-1bf49bce1db74c0fae2fb1376987c77a
- 出典データセット
- uspto-grants-1976_03
- 特許番号
- US03946009
関連ノート
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