1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-bromo-2-chloro-N-(2,2-diethoxyethyl)benzamide
反応式
[Cl:1][C:2]1[CH:10]=[C:9]([Br:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[CH2:12]([O:14][CH:15]([O:18][CH2:19][CH3:20])[CH2:16][NH2:17])[CH3:13].CCN=C=NCCCN(C)C>C(Cl)Cl>[Br:11][C:9]1[CH:8]=[CH:7][C:3]([C:4]([NH:17][CH2:16][CH:15]([O:18][CH2:19][CH3:20])[O:14][CH2:12][CH3:13])=[O:6])=[C:2]([Cl:1])[CH:10]=1参加物
5
実験手順
To a suspension of 2-chloro-4-bromobenzoic acid (10.0 g, 42.47 mmol) in CH2Cl2 (1000 mL) was added aminoacetaldehyde diethyl acetal (5.1 mL, 46.72 mmol) and WSC (9.77 g, 50.96 mmol) at room temperature, and stirred for 4 hours. The mixture was washed with water (100 mL), dried over MgSO4. Removal of the solvent, gave title compound (14.88 g, 100% yield).
後処理
- washThe mixture was washed with water (100 mL)
- dry with materialdried over MgSO4
- customRemoval of the solvent
出典と根拠
- ORDレコード
- ord-9971407d6b864fc4865cbb0413c988fb
- 出典データセット
- uspto-grants-2003_08
- 特許番号
- US06603008B1
反応ノート
読み込み中…