Chloroacetic Acid → 5-Methoxyuracil
反応式
[CH3:1][O:2][C:3]1[C:4](=[O:10])[NH:5][C:6](=S)[NH:7][CH:8]=1.ClCC(O)=[O:14].Cl>O>[CH3:1][O:2][C:3]1[C:4](=[O:10])[NH:5][C:6](=[O:14])[NH:7][CH:8]=1参加物
5
実験手順
A mixture of 5-(methoxy)-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone (21.5 g; 0.137 moles), chloroacetic acid (21.5 g; 0.227 moles), and water (585 mL) was refluxed for 2 h. Concentrated HCl (85 mL) was added and the mixture was then refluxed for 16 h. Upon cooling, a solid formed and was collected by filtration, washed with water and dried to yield the desired product (18.2 g; 94% yield). MS: (M+H)+=143.
後処理
- temperaturewas refluxed for 2 h
- temperaturethe mixture was then refluxed for 16 h
- temperatureUpon cooling
- customa solid formed
- filtrationwas collected by filtration
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-3f6c6f12a8b34b6e8abec49dc8090da2
- 出典データセット
- uspto-grants-2009_12
- 特許番号
- US07625903B2
反応ノート
読み込み中…