HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47099Erstellt: 23. Oktober 2026
2,5-Hexanedione → 3-Sulphamoyl-4-phenoxy-5-[beta-(2,5-dimethyl-1-pyrrolyl)-ethyl]-benzoic acid
https://huagongshe.com/de/reaction/47099
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,5-Hexanedione | HCID 8035 | — |
| Edukt | Aluminum | HCID 5359268 | — |
| Edukt | 3-Sulphamoyl-4-phenoxy-5-[beta-aminoethyl]-benzoic acid | HCID 12795717 | — |
| Lösungsmittel | Hexamethylphosphoramide | HCID 12679 | — |
| Produkt | 3-Sulphamoyl-4-phenoxy-5-[beta-(2,5-dimethyl-1-pyrrolyl)-ethyl]-benzoic acid | HCID 13021084 | — |
Reaktionsschritte
A mixture of 3-sulphamoyl-4-phenoxy-5-[β-aminoethyl]-benzoic acid (5.0 g=1.35 mmols; see Example 3 for the preparation), acetonylacetone (1.85 g, approximately 16.2 mmols) and hexamethylphosphoric acid triamide (Hexametapol; 25 ml) is warmed at 100° for 30 minutes under N2 in an apparatus which has been protected against incident light by covering it with aluminium foil, and the reaction solution is worked up as follows, with strict exclusion of light throughout: pouring into ice-water (50 ml) and extracting with ethyl acetate, washing the extract with water, drying and filtering and evaporating the filtrate. The crude product is recrystallised from chloroform/cyclohexane with the addition of active charcoal and gives pale orange-coloured, light-sensitive crystals, melting point>210° (decomposition).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04176190 |
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| Quelldatensatz | uspto-grants-1979_11 |
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| ORD ID | ord-970005fb4a7e42419affa6245d0b5231 |
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| Quellennotiz | uspto-grants-1979_11 |
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