Lithium Hydroxide → 1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid
反応式
C([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]([C:17]([CH3:20])([CH3:19])[CH3:18])[C:10]=1[C:11]1[CH:15]=[C:14]([Cl:16])[O:13][N:12]=1)=[O:5])C.[OH-].[Li+]>C(O)C>[C:17]([N:9]1[C:10]([C:11]2[CH:15]=[C:14]([Cl:16])[O:13][N:12]=2)=[C:6]([C:4]([OH:5])=[O:3])[CH:7]=[N:8]1)([CH3:20])([CH3:18])[CH3:19]参加物
4
反応条件
- 温度
- 25 °C
実験手順
A solution of 1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (55.3 mg, 0.18 mmol) in absolute ethanol (0.93 mL, 0.2M) was treated with a 2M aqueous lithium hydroxide solution (0.18 mL, 0.37 mmol). The reaction was stirred at 25° C. for 1.5 h and then was heated to 100° C. for 1 h. At this time, the reaction was allowed to cool to 25° C. and was stirred at 25° C. overnight. At this time, the reaction was concentrated in vacuo. The residue was treated with water followed by acidification to pH=1 with a 1N aqueous hydrochloric acid solution. The resulting precipitate that formed was collected by filtration, washed with water and hexanes and dried in vacuo to afford 1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid (38.7 mg, 77%) as an off-white solid.