Citric Acid → 4-Tert-butoxycarbonylamino-4-cyclohexyl-butyric acid
反応式
C[O:2][C:3](=[O:21])[CH2:4][CH2:5][CH:6]([NH:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1.[OH-].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CO>[C:17]([O:16][C:14]([NH:13][CH:6]([CH:7]1[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12]1)[CH2:5][CH2:4][C:3]([OH:21])=[O:2])=[O:15])([CH3:20])([CH3:18])[CH3:19]参加物
5
実験手順
To a solution of 4-tert-butoxycarbonylamino-4-cyclohexyl-butyric acid methyl ester (9 g) in MeOH (100 mL) was added 1N NaOH (31 mL) and the reaction mixture was stirred at room temperature overnight. Citric acid (7 g) was then added, and the MeOH was removed under vacuum. The product was extracted with EtOAc (300 mL). The organic layer was washed with aqueous NaCl solution, dried with MgSO4, and evaporated to yield 4-tert-butoxycarbonylamino-4-cyclohexyl-butyric acid as an off white solid.
後処理
- customthe MeOH was removed under vacuum
- extractionThe product was extracted with EtOAc (300 mL)
- washThe organic layer was washed with aqueous NaCl solution
- dry with materialdried with MgSO4
- customevaporated
出典と根拠
- ORDレコード
- ord-d671e0b59aa54f6caa12e46fe0741f0f
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07531545B2
反応ノート
読み込み中…