反応式
FC1C=CC([N+]([O-])=O)=CC=1.N1C=NN=N1.C(=O)([O-])[O-].[K+].[K+].N1(C2C=CC([N+]([O-])=O)=CC=2)C=NN=N1.[N:36]1[N:37]([C:41]2[CH:46]=[CH:45][C:44]([N+:47]([O-])=O)=[CH:43][CH:42]=2)[N:38]=[N:39][CH:40]=1>CN(C=O)C.C1COCC1.[Pt](=O)=O.O>[N:36]1[N:37]([C:41]2[CH:46]=[CH:45][C:44]([NH2:47])=[CH:43][CH:42]=2)[N:38]=[N:39][CH:40]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 4
反応条件
- 温度
- 80 °C
実験手順
To a solution of 4-fluoro-1-nitrobenzene (12.5 g, 89 mmol) and 1H-tetrazole (6.21 g, 89 mmol) in DMF (89 mL) stirred at room temperature, potassium carbonate (12.24 g, 89 mmol) was added in one portion. The resulting mixture was stirred at 80° C. overnight, and then reaction mixture was worked up by the addition of water at 80° C., then cooled to room temperature, and stirred at room temperature for 30 minutes. The yellow solid was collected by filtration, washed with water, air-dried for 2 hours, and dried in an vacuum oven at 60° C. for 2 hours to afford a mixture of 4-(1H-tetrazol-1-yl)-1-nitrobenzene and 4-(2H-tetrazol-2-yl)-1-nitrobenzene. The product thus obtained was re-dissolved in THF (209 mL) and, while stirring at room temperature, platinum(IV) oxide (0.45 g, 1.982 mmol) was added in one portion. The resulting mixture was stirred at room temperature overnight under a hydrogen atmosphere, after which the reaction mixture was worked up by filtration through a celite pad and the solvent removed by evaporation. The residue was purified and separated by CombiFlash® (0-50% EtOAc/toluene; Teledyne Isco, Inc., Lincoln, Nebr.) to afford the desired 4-(2H-tetrazol-2-yl)aniline as a yellowish solid. 1H NMR (400 MHz, DMSO-d6): δ 9.08 (s, 1H), 7.72 (d, 2H), 6.73 (d, 2H), 5.75 (s, 2H).
後処理
- customreaction mixture
- temperaturecooled to room temperature
- stirringstirred at room temperature for 30 minutes
- filtrationThe yellow solid was collected by filtration
- washwashed with water
- customair-dried for 2 hours
- customdried in an vacuum oven at 60° C. for 2 hours
- customto afford
- customThe product thus obtained
- stirringwhile stirring at room temperature
- stirringThe resulting mixture was stirred at room temperature overnight under a hydrogen atmosphere
- filtrationafter which the reaction mixture was worked up by filtration through a celite pad
- customthe solvent removed by evaporation
- customThe residue was purified
- customseparated by CombiFlash® (0-50% EtOAc/toluene; Teledyne Isco, Inc., Lincoln, Nebr.)
出典と根拠
- ORDレコード
- ord-ab33d0c5c1ee46eba7d23664771c01c1
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09133157B2
関連ノート
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