反応式
[Cl:1]N1C(=O)CCC1=O.[CH3:9][C:10]1[C:16]([CH3:17])=[CH:15][CH:14]=[CH:13][C:11]=1[NH2:12]>CN(C=O)C>[CH3:9][C:10]1[C:16]([CH3:17])=[CH:15][CH:14]=[C:13]([Cl:1])[C:11]=1[NH2:12]参加物
4
実験手順
used in the preparation of 389 was prepared as follows: N-Chlorosuccinimide (1.00 g; 8.2 mmol) was added to a solution of 2,3-dimethylaniline (1 ml; 8.2 mmol) in 20 ml of DMF in the dark. After stirring 1 hr. in the dark, the reaction mixture was partitioned between EtOAc (100 ml) and water (100 ml). The organic layer was washed with 1N NaOH (100 ml), water (100 ml) and brine (50 ml). Drying (MgSO4) and concentration afforded 1.25 g (99%) of 2,3-dimethyl-6-chloroaniline as a deep red liquid.
後処理
- customwas prepared
- customin the dark, the reaction mixture was partitioned between EtOAc (100 ml) and water (100 ml)
- washThe organic layer was washed with 1N NaOH (100 ml), water (100 ml) and brine (50 ml)
- customDrying
- concentration(MgSO4) and concentration
出典と根拠
- ORDレコード
- ord-b0cb638d6a32473e867ac1465c30ef9d
- 出典データセット
- uspto-grants-2001_05
- 特許番号
- US06235740B1
関連ノート
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