反応式
Cl[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][CH:6]=1)=[O:4].[NH:12]1[CH:16]=[N:15][CH:14]=[N:13]1.C(N(CC)CC)C.O>C(#N)C>[N:12]1([CH2:2][C:3]([C:5]2[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][CH:6]=2)=[O:4])[CH:16]=[N:15][CH:14]=[N:13]1参加物
6
実験手順
2,4'-Dichloroacetophenone (0.03 mol) and 1,2,4-triazole (0.03 mol) were suspended in acetonitrile (50 ml) and cooled to -20°. Triethylamine (0.03 mol) was added dropwise with stirring. After stirring at -20° for 2 hours, the mixture was poured into water, and the product filtered off, washed with water, dried and crystallised from toluene to give pale yellow needles of 2-(1,2,4-triazol-1-yl)-4'-chloroacetophenone, m.p. 151°-3°.
後処理
- temperaturecooled to -20°
- stirringAfter stirring at -20° for 2 hours
- filtrationthe product filtered off
- washwashed with water
- customdried
- customcrystallised from toluene
出典と根拠
- ORDレコード
- ord-6e4a31fa96d74d9b992f0fcf7abbd637
- 出典データセット
- uspto-grants-1979_04
- 特許番号
- US04147793
関連ノート
読み込み中…