反応式
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:3]=1[C:4](O)=[O:5].C(O)(=O)C.[O:16]([C:18]#[N:19])[Na].[OH-].[Na+]>O>[Cl:11][C:8]1[CH:7]=[C:3]2[C:2](=[CH:10][CH:9]=1)[NH:1][C:18](=[O:16])[NH:19][C:4]2=[O:5]参加物
6
反応条件
- 温度
- 30 °C
実験手順
Into a 500-mL 3-necked round-bottom flask, was placed a solution of 2-amino-5-chlorobenzoic acid (10 g, 58.48 mmol, 1.00 equiv) in water (100 mL), acetic acid (8 g, 133.33 mmol, 2.24 equiv). This was followed by the addition of NaOCN (8.2 g, 126.15 mmol, 2.13 equiv). The mixture was stirred for 30 mins at 30° C. To this was added sodium hydroxide (86 g, 2.15 mol, 37.00 equiv). The resulting solution was stirred overnight at 30° C. The solids were collected by filtration. The residue was dissolved in water. The pH value of the solution was adjusted to 7 with hydrogen chloride (12 mol/L). The solids were collected by filtration. This resulted in 5 g (44%) of 6-chloroquinazoline-2,4(1H,3H)-dione as a white solid.
後処理
- customInto a 500-mL 3-necked round-bottom flask, was placed
- stirringThe resulting solution was stirred overnight at 30° C
- filtrationThe solids were collected by filtration
- dissolutionThe residue was dissolved in water
- filtrationThe solids were collected by filtration
- customThis resulted in 5 g (44%) of 6-chloroquinazoline-2,4(1H,3H)-dione as a white solid
出典と根拠
- ORDレコード
- ord-a0a831190e1f4b5e9848c1c3b2620b18
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08541448B2
関連ノート
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