Ammonium Hydroxide → 3-Hydroxy-3-methylglutaric acid monoamide, ammonium salt
反応式
[OH:1][C:2]1([CH3:10])[CH2:8][C:7](=[O:9])[O:6][C:4](=[O:5])[CH2:3]1.[OH-].[NH4+:12]>>[NH4+:12].[OH:1][C:2]([CH3:10])([CH2:8][C:7]([O-:6])=[O:9])[CH2:3][C:4]([NH2:12])=[O:5]参加物
3
実験手順
1.7 g. (0.011 moles) of 3-hydroxy-3-methylglutaric acid anhydride (prepared according to the method of Hilz, et al, Biochem Zeit, 329, 476-489 (1958)) in 30 ml of 15 N ammonium hydroxide is allowed to stand at 25° C. for 10 minutes. The solution is then evaporated to dryness under vacuum and the resulting residue dissolved in 10 ml of warm methanol. Ethyl acetate (10 ml) is then slowly added to the methanol solution. Upon cooling, 1.5 g. of 3-hydroxy-3-methylglutaric acid monoamide, ammonium salt is obtained as a white crystalline solid.
後処理
- customThe solution is then evaporated to dryness under vacuum
- dissolutionthe resulting residue dissolved in 10 ml of warm methanol
- additionEthyl acetate (10 ml) is then slowly added to the methanol solution
- temperatureUpon cooling
出典と根拠
- ORDレコード
- ord-df7f9b89d17546a5b91da40096676264
- 出典データセット
- uspto-grants-1980_06
- 特許番号
- US04208204
反応ノート
読み込み中…