反応式
[CH3:1][N:2]1[CH:6]=[C:5]([C:7]([O:9]CC)=[O:8])[CH:4]=[N:3]1.[OH-].[Na+]>C(O)C>[CH3:1][N:2]1[CH:6]=[C:5]([C:7]([OH:9])=[O:8])[CH:4]=[N:3]1参加物
4
実験手順
A solution of ethyl 1-methyl-1H-pyrazole-4-carboxylate (20.2 g, 131 mmol) and NaOH (6.3 g, 158 mmol) in 200 mL absolute ethanol was refluxed for 2 h and stirring was continued at RT for 18 h. After that, the solvent was removed in vacuo. The residue was dissolved in water. The aq solution was washed with ether and acidified with concentrated HCl. The solid was filtered, washed with water and air-dried to give 14.2 g of 1-methyl-1H-pyrazole-4-carboxylic acid in 86% yield.
後処理
- customAfter that, the solvent was removed in vacuo
- dissolutionThe residue was dissolved in water
- washThe aq solution was washed with ether
- filtrationThe solid was filtered
- washwashed with water
- customair-dried
出典と根拠
- ORDレコード
- ord-678b8f3e661843e1a2cc3f135a8dd846
- 出典データセット
- uspto-grants-2000_10
- 特許番号
- US06133252
関連ノート
読み込み中…