反応式
ClC1C=C(Cl)C(Cl)=CC=1N.Cl.N([O-])=O.[Na+].[O:16]=[C:17]1[CH2:22][CH2:21][CH2:20][CH2:19][CH:18]1[C:23]([O:25]CC)=[O:24].[OH-].[Na+]>O>[O:16]=[C:17]1[CH2:22][CH2:21][CH2:20][CH2:19][CH:18]1[C:23]([OH:25])=[O:24]参加物
反応条件
- 温度
- 0 °C
実験手順
To a solution of 2,4,5-trichloroaniline (2.48 g, 12.6 mmol) in H2O (5 mL), cooled to 0° C., conc. HCl (7.5 mL) was added, and then stirred for 20 min. NaNO2 (0.87 g, 12.0 mmol) dissolved in water (5 mL), was added slowly and the reaction was continued at 0° C. for 1 h, filtered and the filtrate was used further. In another setup, ethyl 2-oxocyclohexanecarboxylate (2.0 g, 12.0 mmol) was added to 5N NaOH (0.56 g) and stirred for 16 h. The reaction mixture was cooled to 0° C., conc. HCl (1.2 mL) was added slowly, stirred for another 45 min. to obtain 2-oxocyclohexanecarboxylic acid which was added to the filtrate (prepared above) at 0° C. The resulting yellow solid precipitate was filtered, air dried to give the title compound (1.7 g, 44%) which was used in the next step without any spectroscopic analysis.
後処理
- additionwas added slowly
- waitthe reaction was continued at 0° C. for 1 h
- filtrationfiltered
- stirringstirred for 16 h
- stirringstirred for another 45 min.
出典と根拠
- ORDレコード
- ord-abdaac3e628b4d67a4222c8d68300ce8
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08987319B2
関連ノート
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