Thionyl Chloride → 4-(1H-1,2,4-Triazol-1-yl)benzoyl chloride
反応式
[N:1]1([C:6]2[CH:14]=[CH:13][C:9]([C:10](O)=[O:11])=[CH:8][CH:7]=2)[CH:5]=[N:4][CH:3]=[N:2]1.S(Cl)([Cl:17])=O>>[N:1]1([C:6]2[CH:14]=[CH:13][C:9]([C:10]([Cl:17])=[O:11])=[CH:8][CH:7]=2)[CH:5]=[N:4][CH:3]=[N:2]1参加物
3
実験手順
4-(1H-1,2,4-triazol-1-yl)benzoic acid (100 mg, 0.529 mmol) in sulfurous dichloride (2 ml) was refluxed at 110° C. for 2 h. After the excess SOCl2 was removed, the residue was dried in vacuo to give 4-(1H-1,2,4-triazol-1-yl)benzoyl chloride (110 mg, 0.529 mmol, 100% yield) as a white solid which was used in subsequent reactions without further purification.
後処理
- customAfter the excess SOCl2 was removed
- customthe residue was dried in vacuo
出典と根拠
- ORDレコード
- ord-abd5d89a47484141a88643f312bcc924
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08362004B2
反応ノート
読み込み中…