Hydrochloric Acid → 3-Cyclopropyl-1,2-oxazole-4-carboxylic acid
反応式
C([O:3][C:4]([C:6]1[C:7]([CH:11]2[CH2:13][CH2:12]2)=[N:8][O:9][CH:10]=1)=[O:5])C.[OH-].[K+].Cl>C(O)C.O.O>[CH:11]1([C:7]2[C:6]([C:4]([OH:5])=[O:3])=[CH:10][O:9][N:8]=2)[CH2:12][CH2:13]1参加物
6
実験手順
5.6 g (31 mmol) of 3-Cyclopropyl-isoxazole-4-carboxylic acid ethyl ester were slowly added to a solution of 6.1 g (93 mmol, 85% purity) of potassium hydroxide in ethanol/water (1:3, 100 ml) at 0° C. The reaction mixture was stirred at room temperature for 16 h, diluted with water, acidified (pH=2) with 20% aqueous HCl and extracted with dichloromethane. The combined organic layers were dried over sodium sulfate, filtered and the solvent was removed to yield 4.7 g (94%, 95% purity) of the title compound which did not need further purification.
後処理
- extractionextracted with dichloromethane
- dry with materialThe combined organic layers were dried over sodium sulfate
- filtrationfiltered
- customthe solvent was removed
出典と根拠
- ORDレコード
- ord-53b075df594b4885bcb304873d7abb92
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09125414B2
反応ノート
読み込み中…