反応式
[Cl:1][C:2]1[CH:7]=[C:6](Cl)[CH:5]=[C:4]([Cl:9])[N:3]=1.[CH3:10][NH2:11]>C(O)C>[Cl:1][C:2]1[CH:7]=[C:6]([NH:11][CH3:10])[CH:5]=[C:4]([Cl:9])[N:3]=1参加物
4
反応条件
- 温度
- 22.5 °C
実験手順
2,4,6-Trichloropyridine (1800 g, 9.89 mol) was dissolved in ethanol (1800 mL). Methylamine 40% solution in ethanol (6.3 L) was added over 1 h and 40 min maintaining the reaction temperature between 20-25° C. The reaction was stirred for 14 hours at room temperature and concentrated. The product was filtered, washed with methyl t-butyl ether (1,500 ml) and dried to yield A1.6 (1200 g, 68%)
後処理
- concentrationconcentrated
- filtrationThe product was filtered
- washwashed with methyl t-butyl ether (1,500 ml)
- customdried
- customto yield A1.6 (1200 g, 68%)
出典と根拠
- ORDレコード
- ord-336a37a99c754ec081c44405c93b39d8
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07737279B2
関連ノート
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