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HRID 263153作成日:2026年10月24日

Hydrochloric Acid → 3-Chloro-5-(3-fluorosulfonylphenylazo)-2-hydroxy benzaldehyde

https://huagongshe.com/ja/reaction/263153

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Benzenesulfonyl fluoride, 3-amino-, hydrochloride (1:1)HCID 77496—
反応物3-Chloro-2-hydroxybenzaldehydeHCID 519651—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物3-Chloro-5-(3-fluorosulfonylphenylazo)-2-hydroxy benzaldehydeHCID 135677442—

反応条件

温度0 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04156609
出典データセットuspto-grants-1979_05
ORD IDord-1ec54e38ca794699aaba96952205f042
出典メモuspto-grants-1979_05