反応式
[NH2:1][CH2:2][C:3]([NH:5][CH2:6][C:7]([OH:9])=[O:8])=[O:4].[C:10](Cl)(=[O:14])[C:11]([CH3:13])=[CH2:12]>O>[C:10]([NH:1][CH2:2][C:3]([NH:5][CH2:6][C:7]([OH:9])=[O:8])=[O:4])(=[O:14])[C:11]([CH3:13])=[CH2:12]参加物
4
実験手順
Using Example 1, glycylglycine was reacted with methacryloyl chloride in water at -10° C. After adjustment to a pH of 3, the white slurry was washed with ethanol to remove sodium chloride and water. The product was dried at 80° C. to obtain a good yield (>75%) product with a melting point of 200°-201° C.
後処理
- washAfter adjustment to a pH of 3, the white slurry was washed with ethanol
- customto remove sodium chloride and water
- customThe product was dried at 80° C.
- customto obtain
出典と根拠
- ORDレコード
- ord-86af07b8d12f4df8a95f65f97388eba5
- 出典データセット
- uspto-grants-1994_11
- 特許番号
- US05369142
関連ノート
読み込み中…