HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 918667Erstellt: 25. Oktober 2026
p-Toluenesulfonic acid → HCID 21506067, Verbindung
https://huagongshe.com/reaction/918667
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Piperonal | HCID 8438 | — |
| Edukt | 3-Amino-4-phenoxy-5-sulfamoylbenzoic acid | HCID 119927 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Platinum oxide (PtO) | HCID 82844 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | HCID 21506067 | HCID 21506067 | — |
Reaktionsschritte
To a suspension of 3-amino-4-phenoxy-5-sulphamyl-benzoic acid (1.54 g) in acetic acid (30 ml), piperonal (0.75 g) was added. After the addition of platinum oxide (25 mg) and a catalytic amount of p-toluenesulphonic acid, the reaction mixture was hydrogenated at room temperature and 1.1 atmospheres hydrogen pressure until the hydrogen uptake had become negligible. Then the reaction mixture was filtered by suction. The filter cake was suspended in water (100 ml), and the pH was adjusted to 8.5 by addition of lithium hydroxide. After the catalyst had been removed from the resulting solution, the 3-(3,4-methylenedioxybenzylamino)-4-phenoxy-5-sulphamyl-benzoic acid was precipitated from the filtrate by addition of 4N hydrochloric acid until the pH was 3. After recrystallization from methanol, the melting point was 229°-230°C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03971819 |
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| Quelldatensatz | uspto-grants-1976_07 |
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| ORD ID | ord-838e789611c743989ca0ae934ebf6d6b |
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| Quellennotiz | uspto-grants-1976_07 |
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