反応式
C[O:2][C:3]([C:5]1[CH:9]=[C:8]([C:10]2[N:11]=[CH:12][O:13][CH:14]=2)[S:7][CH:6]=1)=[O:4].[OH-].[Na+]>>[O:13]1[CH:14]=[C:10]([C:8]2[S:7][CH:6]=[C:5]([C:3]([OH:4])=[O:2])[CH:9]=2)[N:11]=[CH:12]1参加物
3
実験手順
5-Oxazol-4-yl-thiophene-3-carboxylic acid methyl ester (0.049 g, 0.23 mmol) was suspended in IMS (1 mL), sodium hydroxide (1 M, 0.35 mL) was added and the mixture stirred for 60 hours at room temperature. The mixture was quenched with HCl (1 N, 0.35 mL) and then concentrated, azeotroping twice with methanol to afford 5-oxazol-4-yl-thiophene-3-carboxylic acid as a white solid (0.045 g).
後処理
- customThe mixture was quenched with HCl (1 N, 0.35 mL)
- concentrationconcentrated
- customazeotroping twice with methanol
出典と根拠
- ORDレコード
- ord-c7de7615fddd4f519cf036cba9e59553
- 出典データセット
- uspto-grants-2013_12
- 特許番号
- US08614209B2
関連ノート
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