6-Methyluracil → 5-Fluoro-6-methylpyrimidine-2,4-diol
反応式
[CH3:1][C:2]1[NH:7][C:6](=[O:8])[NH:5][C:4](=[O:9])[CH:3]=1.[F:10]F>O>[F:10][C:3]1[C:4](=[O:9])[NH:5][C:6](=[O:8])[NH:7][C:2]=1[CH3:1]参加物
4
実験手順
The preceding example was substantially repeated but at a lower reaction temperature. A suspension of 6-methyl uracil (4.00g) in water (30 ml) was maintained at 0°-10°C and fluorinated with a stream of fluorine and nitrogen, present in equal volumes, until fluorine was detected at the reactor outlet. The reaction mixture was allowed to stand for two days at room temperature and 1.05g of crystals were collected and found to have a different IR spectrum than the starting material. A DSC analysis showed 2 transitions at 313°C and 318°C followed by apparent decomposition. The structure of the product was identified as 5-fluoro-6-methyl uracil by NMR analysis.
後処理
- temperaturewas maintained at 0°-10°C
- custom1.05g of crystals were collected
- customat 313°C
- custom318°C
出典と根拠
- ORDレコード
- ord-e0e30c37034847b09d50279a7227833d
- 出典データセット
- uspto-grants-1976_05
- 特許番号
- US03954758
反応ノート
読み込み中…