反応式
[CH3:1][C:2]([CH3:12])([CH3:11])[C:3](=[O:10])[CH2:4][N:5]1[CH:9]=[N:8][CH:7]=[N:6]1.CO[CH:15](OC)[N:16]([CH3:18])[CH3:17]>>[CH3:1][C:2]([CH3:12])([CH3:11])[C:3](=[O:10])[C:4]([N:5]1[CH:9]=[N:8][CH:7]=[N:6]1)=[CH:15][N:16]([CH3:18])[CH3:17]参加物
3
実験手順
250.8 g (1.5 mol) of 3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one and 196 g (1.65 mol) of dimethylformamide dimethyl acetal were heated under reflux for 5 hours. Thereafter, the excess acetal was distilled off. 306 g (92% of theory) of 4,4-dimethyl-1-dimethylamino-2-(1,2,4-triazol-1-yl)-pent-1-en-3-one of refractive index nD20 1.531 were obtained. ##STR14##
後処理
- temperatureunder reflux for 5 hours
- distillationThereafter, the excess acetal was distilled off
出典と根拠
- ORDレコード
- ord-92f219932e104d4e96b8cc1fe3ba899d
- 出典データセット
- uspto-grants-1983_04
- 特許番号
- US04380628
関連ノート
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