Hydrochloric Acid → 2-(1H-1,2,4-triazol-5-yl)aniline
反応式
ClC1[N:11]2[CH:12]=[N:13][N:14]=[C:10]2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1.[OH-].[K+].Cl>>[NH2:3][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:9]=1[C:10]1[NH:14][N:13]=[CH:12][N:11]=1参加物
4
実験手順
To a flask containing 40 gms. of 5-chloro-1,2,4-triazolo[4,3-c]quinazoline is added 800 ml. of a 10% KOH solution and the resulting mixture heated to reflux. A gentle reflux is maintained overnight after which time the mixture is neutralized to pH 7.0 with cooling and stirring by adding dropwise a 1:1 HCl solution and the resulting precipitate filtered off. The aqueous layer is washed 3 or 4 times with methylene chloride, dried and evaporated in vacuo to dryness. The residue is recrystallized from benzene/ether to obtain 5-(2-aminophenyl)-s-triazole, m.p. 145°-148° C.
後処理
- additionTo a flask containing 40 gms
- temperatureA gentle reflux
- temperatureis maintained overnight after which time the mixture
- temperaturewith cooling
- filtrationthe resulting precipitate filtered off
- washThe aqueous layer is washed 3 or 4 times with methylene chloride
- customdried
- customevaporated in vacuo to dryness
- customThe residue is recrystallized from benzene/ether
出典と根拠
- ORDレコード
- ord-0c19ddd929e045959af9dd02dd197fed
- 出典データセット
- uspto-grants-1977_04
- 特許番号
- US04020083
反応ノート
読み込み中…