1H-1,2,4-Triazole → 1-(4-Methoxybenzyl)-1,2,4-triazole
反応式
[NH:1]1[CH:5]=[N:4][CH:3]=[N:2]1.[CH3:6][O:7][C:8]1[CH:15]=[CH:14][C:11]([CH2:12]Cl)=[CH:10][CH:9]=1.C1CCN2C(=NCCC2)CC1>C1COCC1>[CH3:6][O:7][C:8]1[CH:15]=[CH:14][C:11]([CH2:12][N:1]2[CH:5]=[N:4][CH:3]=[N:2]2)=[CH:10][CH:9]=1参加物
5
実験手順
To 1,2,4-triazole (2.0 g, 29 mmol) in THF (80 mL) at 0° C. was added 4-methoxybenzyl chloride (4.0 mL, 29 mmol) and DBU (5.20 mL, 34.7 mmol). The reaction mixture was warmed to room temperature and allowed to stir overnight. The solution was filtered and the filtrate was concentrated. The resulting residue was purified by column chromatography (EtOAc/MeOH, 1:9) to give 3.12 g (57%) of 1-(4-methoxybenzyl)-1H-1,2,4-triazole as a colorless oil.
後処理
- filtrationThe solution was filtered
- concentrationthe filtrate was concentrated
- customThe resulting residue was purified by column chromatography (EtOAc/MeOH, 1:9)
出典と根拠
- ORDレコード
- ord-ad67110a16d7408c8de6eff2bf355f35
- 出典データセット
- uspto-grants-2008_07
- 特許番号
- US07399778B2
反応ノート
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