反応式
[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[C:6]([C:13](Cl)=[O:14])[CH:5]=1.C([O-])([O-])=O.[K+].[K+].[CH3:23][O:24][CH:25]([O:28][CH3:29])[CH2:26][NH2:27]>C(Cl)Cl.C(OCC)(=O)C>[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[C:6]([C:13]([NH:27][CH2:26][CH:25]([O:28][CH3:29])[O:24][CH3:23])=[O:14])[CH:5]=1参加物
6
実験手順
Under ice cooling a solution of 22.1 g (90.7 mmol) of 3-chlorocarbonyl-5-nitro-benzoic acid methyl ester (U.S. Pat. No. 4,120,891) in 200 ml of DCM is added dropwise to a stirred suspension of 11.2 g (181 mmol) of K2CO3 and 11.7 ml (109 mmol) of aminoacetaldehyde dimethylacetal in 200 ml of DCM. The mixture is stirred at ambient temperature for 2 days, diluted with ethyl acetate and extensively washed with water. The organic phase is dried over sodium sulfate and evaporated to yield the product in the form of a yellow oil.
後処理
- washextensively washed with water
- dry with materialThe organic phase is dried over sodium sulfate
- customevaporated
- customto yield the product in the form of a yellow oil
出典と根拠
- ORDレコード
- ord-5168e8333bb54d3397d3ae3a4e195b8b
- 出典データセット
- uspto-grants-2011_10
- 特許番号
- US08039455B2
関連ノート
読み込み中…