反応式
C[O:2][C:3]([C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]([CH3:14])[N:6]=1)=[O:4].[OH-].[Na+]>O1CCCC1>[CH3:14][N:7]1[C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:5]([C:3]([OH:4])=[O:2])=[N:6]1参加物
4
実験手順
Methyl-1-methylindazole-3-carboxylate (3.1 g, 0.016 mol) was stirred with a solution of sodium hydroxide (0.78 g, 0.02 mol) in tetrahydrofuran (100 ml) for 2 hours at room temperature, the solution evaporated and the yellow residue were dissolved in water. Acidification with methanesulfonic acid precipitated 1-methylindazole-3-carboxylic acid (2.19 g). A further crop (0.3 g) was obtained by extraction of the aqueous acid solution with a mixture of ether and methylene chloride. Total yield 2.49 g (87%).
後処理
- customthe solution evaporated
- dissolutionthe yellow residue were dissolved in water
- customAcidification with methanesulfonic acid precipitated 1-methylindazole-3-carboxylic acid (2.19 g)
- customA further crop (0.3 g) was obtained by extraction of the aqueous acid solution with a mixture of ether and methylene chloride
出典と根拠
- ORDレコード
- ord-2aceac8fd9bc48ee985d35fc94fba092
- 出典データセット
- uspto-grants-1999_09
- 特許番号
- US05955470
関連ノート
読み込み中…