反応式
[CH2:1]([C:3]1[N:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:6]([C:14]2[CH:19]=[CH:18][C:17]([O:20]C)=[CH:16][CH:15]=2)=[N:5][N:4]=1)[CH3:2]>Br>[CH2:1]([C:3]1[N:7]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:6]([C:14]2[CH:15]=[CH:16][C:17]([OH:20])=[CH:18][CH:19]=2)=[N:5][N:4]=1)[CH3:2]参加物
実験手順
A solution of 3.86 g of 3-ethyl-5-(4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole and 20 ml of a hydrobromic acid solution at 48% was refluxed with stirring for one hour and the mixture was evaporated to dryness under reduced pressure. The residue was dissolved in 20 ml of hot water and ammonium hydroxide was added until the pH was alkaline. The mixture was stood overnight with stirring and was vacuum. The product was washed with water and dried at 90° C. under reduced pressure. The 3.65 g of product were crystallized from methanol and the mixture was iced and vacuum filtered. The crystals were washed by empasting with methanol and were dried at 90° C. under reduced pressure to obtain 3.245 g of 4-(3-ethyl-4-phenyl-4H-1,2,4-triazol-5-yl)-phenol melting at 275° C.
後処理
- customthe mixture was evaporated to dryness under reduced pressure
- dissolutionThe residue was dissolved in 20 ml of hot water
- additionammonium hydroxide was added until the pH
- waitThe mixture was stood overnight
- stirringwith stirring
- washThe product was washed with water
- customdried at 90° C. under reduced pressure
- customThe 3.65 g of product were crystallized from methanol
- filtrationvacuum filtered
- washThe crystals were washed
- customwere dried at 90° C. under reduced pressure
出典と根拠
- ORDレコード
- ord-eb288b568d2e414b9efcf337b3879fca
- 出典データセット
- uspto-grants-1987_04
- 特許番号
- US04659729
関連ノート
読み込み中…