Diazomethane → Methyl 8-Hydroxyquinoline-2-Carboxylate
反応式
[OH:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([C:12]([OH:14])=[O:13])[CH:8]=[CH:7]2.[N+](=[CH2:17])=[N-]>O1CCCC1>[OH:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([C:12]([O:14][CH3:17])=[O:13])[CH:8]=[CH:7]2参加物
4
実験手順
8-Hydroxyquinoline-2-carboxylic acid (2.08 g) and tetrahydrofuran (200 ml) were combined and stirred with ice bath cooling. Diazomethane (approx. 16.6 mmol in solution in diethyl ether) was then added and the whole stirred for 1.5 h as it slowly warmed to room temperature. Nitrogen was blown through the reaction mixture to purge any excess diazomethane and the solution was evaporated in vacuo to give the title compound (1.6 g).
後処理
- temperaturecooling
- stirringthe whole stirred for 1.5 h as it
- customto purge any excess diazomethane
- customthe solution was evaporated in vacuo
出典と根拠
- ORDレコード
- ord-4c7b361eae324ebeabfcce85d7c21218
- 出典データセット
- uspto-grants-1998_09
- 特許番号
- US05804588
反応ノート
読み込み中…