反応式
[Cl:1][C:2]([Cl:6])([Cl:5])[C:3]#[N:4].[ClH:7]>>[Cl:1][C:2]([Cl:6])([Cl:5])[C:3]1[N:4]=[C:3]([C:2]([Cl:1])([Cl:7])[Cl:7])[N:4]=[C:3]([C:2]([Cl:6])([Cl:5])[Cl:1])[N:4]=1参加物
3
実験手順
Aluminum bromide (0.5 g, 0.0019 mol) was added to a solution of the compound 5a (4.4 g, 0.019 mol) obtained in the above (1) dissolved in trichloroacetonitrile (43 g, 0.298 mol). Dry hydrogen chloride gas was passed through the reaction mixture at −10° C. for 2 hours. Then, the mixture was stirred at room temperature for one day. Trichloroacetonitrile was removed under reduced pressure. The residue was purified by a column (hexane/ethyl acetate=9/1). As a result, the mixture of 2,4-trichloromethyl-(2′-acetylbiphenyl)-6-triazine (5b) and 2,4,6-tris(trichloromethyl)-1,3,5-triazine was obtained. These two products were not separated since they have similar solubility in any solvent.
後処理
- customTrichloroacetonitrile was removed under reduced pressure
- customThe residue was purified by a column (hexane/ethyl acetate=9/1)
- additionAs a result, the mixture of 2,4-trichloromethyl-(2′-acetylbiphenyl)-6-triazine (5b)
出典と根拠
- ORDレコード
- ord-3165f3a3ab614ac5ab032f5904dba123
- 出典データセット
- uspto-grants-2008_11
- 特許番号
- US07449574B2
関連ノート
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