反応式
[C:1]1(=[O:7])O[C:4](=[O:5])[CH:3]=[CH:2]1.[CH2:8]([CH2:13][O:14][CH2:15][CH2:16][NH2:17])[O:9][CH2:10][CH2:11][NH2:12].[C:18]([O-:21])(=O)[CH3:19].[Na+].[C:23](OC(=O)C)(=[O:25])[CH3:24]>>[CH2:13]([O:14][CH2:15][CH2:16][N:17]1[C:1](=[O:7])[CH:2]=[CH:3][C:4]1=[O:5])[CH2:8][O:9][CH2:10][CH2:11][N:12]1[C:18](=[O:21])[CH:19]=[CH:24][C:23]1=[O:25]参加物
5
実験手順
The general procedure was carried out using maleic anhydride (13.23 g, 135 mmol), 2,2′-(ethylenedioxy)bis(ethylamine) (10.0 g, 67.5 mmol), sodium acetate (1.11 g, 13.5 mmol), and acetic anhydride (15.15 g, 148 mmol). The resulting compound was purified by column chromatography (95:5 DCM:EtOAc), and the product obtained as a white solid (4.5 g/22%).
後処理
- customThe resulting compound was purified by column chromatography (95:5 DCM:EtOAc)
- customthe product obtained as a white solid (4.5 g/22%)
出典と根拠
- ORDレコード
- ord-e61e1364dca24f1d9c1dac17ebcc359c
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09193139B2
関連ノート
読み込み中…