反応式
Cl.[NH2:2][C:3]1[CH:4]=[C:5]([S:9]([F:12])(=[O:11])=[O:10])[CH:6]=[CH:7][CH:8]=1.Cl.[N:14]([O-])=O.[Na+].[Cl:18][C:19]1[C:20]([OH:27])=[C:21]([CH:24]=[CH:25][CH:26]=1)[CH:22]=[O:23]>O.N1C=CC=CC=1>[Cl:18][C:19]1[C:20]([OH:27])=[C:21]([CH:24]=[C:25]([N:14]=[N:2][C:3]2[CH:8]=[CH:7][CH:6]=[C:5]([S:9]([F:12])(=[O:11])=[O:10])[CH:4]=2)[CH:26]=1)[CH:22]=[O:23]参加物
反応条件
- 温度
- 0 °C
実験手順
m-Aminobenzenesulfonyl fluoride hydrochloride (21.1 g, 0.099 mol) was slurried in hot 10% HCl (300 ml) and then cooled to 0° C. Sodium nitrite (7.0 g, 0.1 mol) was dissolved in 30 ml water and added dropwise to the acidic solution. Vigorous stirring was required to prevent the slurry from coagulating. The diazonium slurry was then added slowly to 500 ml of pyridine containing 3-chloro-2-hydroxy-benzaldehyde (16.0 g, 0.10 mol) at 0° C. The mixture was stirred 30 minutes and then slowly added to 1500 ml ice and hydrochloric acid. The resulting precipitate coagulated into one lump. The liquid was decanted off and the remaining tarry solid crushed and slurried in 50% HCl. The resulting solid was filtered off, washed with water and air dried, (21.1 g). Upon standing 72 hours, the decanted solution yielded an additional 2.8 g. Yield: 23.8 g (70%).
後処理
- additionadded dropwise to the acidic solution
- stirringThe mixture was stirred 30 minutes
- customThe liquid was decanted off
- customthe remaining tarry solid crushed and slurried in 50% HCl
- filtrationThe resulting solid was filtered off
- washwashed with water and air
- customdried
- customthe decanted solution yielded an additional 2.8 g
出典と根拠
- ORDレコード
- ord-1ec54e38ca794699aaba96952205f042
- 出典データセット
- uspto-grants-1979_05
- 特許番号
- US04156609
関連ノート
読み込み中…