反応式
[CH3:1][N:2]([C:4]([N:6]=[C:7]([NH2:9])[NH2:8])=[NH:5])[CH3:3].Cl.[OH-].[Na+].[C:13]([OH:16])(=[O:15])[CH3:14]>O>[CH3:1][N:2]([C:4]([NH:6][C:7]([NH2:9])=[NH:8])=[NH:5])[CH3:3].[C:13]([O-:16])(=[O:15])[CH3:14]参加物
5
実験手順
5 L of water, 2 kg (1 equivalent) of metformin hydrochloride and 578 g (1.2 equivalents) of sodium hydroxide were added to 10 L reactor, and stirred for 2 hours at room temperature. Then 1 L (1.45 equivalents) of acetic acid was added for 1 hour, and the mixture was stirred overnight at room temperature. The resulting crystal was washed with acetone-water (12:1) mixture, and then acetone, and dried at 60° C. to obtain 1,112 g of metformin acetate (yield: 48.7%).
後処理
- stirringthe mixture was stirred overnight at room temperature
- washThe resulting crystal was washed with acetone-water (12:1) mixture
- dry with materialacetone, and dried at 60° C.
出典と根拠
- ORDレコード
- ord-dec2cd9c4d9a4b31a41e029463ef90e6
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08541474B2
関連ノート
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