反応式
[C:1]1([N:7]2[N:11]=[C:10]3[CH:12]=[CH:13][CH:14]=[CH:15][C:9]3=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[BrH:16].C(O)(=O)C.[Br:21]Br.[OH-].[Na+]>ClCCl.O>[Br:16][C:15]1[C:9]2[C:10](=[N:11][N:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[N:8]=2)[C:12]([Br:21])=[CH:13][CH:14]=1参加物
反応条件
- 温度
- 150 °C
実験手順
2-phenyl-2H-benzotriazole (1.10 g, 5.1 mmol) was placed in a 1-neck 250-mL round bottomed flask. HBr/acetic acid (45% w/v, 20 mL) and bromine (0.79 mL, 15.3 mmol) were added. The flask was connected to a condenser and a scrubber. The mixture was heated in an oil bath at 150° C. for 0.5 hr. The solution was cooled to room temperature. Bromine (0.79 mL, 15.3 mmol) was again added to the reaction mixture and it was again heated to 150° C. for 1 hr. This step was repeated three more times. Water (200 mL) and dichloromethane (200 mL) were added to the reaction mixture followed by aqueous sodium hydroxide (1.5 M) solution to neutralize the acid. The organic layer was separated and dried with MgSO4. The solution was filtered and the solvent concentrated using a rotary evaporator. The solid was further dried under high vacuum at 60° C. for 2 hr. Yield: 78%.
後処理
- customThe flask was connected to a condenser
- temperatureThe solution was cooled to room temperature
- temperaturewas again heated to 150° C. for 1 hr
- customThe organic layer was separated
- dry with materialdried with MgSO4
- filtrationThe solution was filtered
- concentrationthe solvent concentrated
- customa rotary evaporator
- customThe solid was further dried under high vacuum at 60° C. for 2 hr
出典と根拠
- ORDレコード
- ord-551e446261e548cdbeab5520f7647fac
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07714099B2
関連ノート
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