Hydrochloric Acid → 2-Aminomethyl-3-bromo-benzoic acid hydrochloride salt
反応式
C(OC([NH:8][CH2:9][C:10]1[C:18]([Br:19])=[CH:17][CH:16]=[CH:15][C:11]=1[C:12]([OH:14])=[O:13])=O)(C)(C)C.[ClH:20]>C(OCC)C>[ClH:20].[NH2:8][CH2:9][C:10]1[C:18]([Br:19])=[CH:17][CH:16]=[CH:15][C:11]=1[C:12]([OH:14])=[O:13]参加物
4
実験手順
A mixture of 2-(tert-Butoxy carbonylamino-methyl)-3-bromo-benzoic acid (0.188 g, 0.57 mmol) in 2M HCl in diethyl ether (10 ml) was stirred at room temperature for 18 hours. The solvent was removed by evaporation under reduced pressure. The solid was diluted with ethyl acetate/dioxan (1:1) (10 ml) and stirred at room temperature for 1.5 hours. The solid was filtered off and dried to give the title compound (0.02 g, 13%) as a white solid.
後処理
- customThe solvent was removed by evaporation under reduced pressure
- additionThe solid was diluted with ethyl acetate/dioxan (1:1) (10 ml)
- stirringstirred at room temperature for 1.5 hours
- filtrationThe solid was filtered off
- customdried
出典と根拠
- ORDレコード
- ord-b774302d34564f4f959dcda875fed9f7
- 出典データセット
- uspto-grants-2006_05
- 特許番号
- US07053122B2
反応ノート
読み込み中…