HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1667355Erstellt: 24. Oktober 2026
4-Hydrazinobenzenesulfonic acid → 6-(2,3-dimethyl-5-sulfo-3H-indol-3-yl)hexanoic acid
https://huagongshe.com/de/reaction/1667355
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Hydrazinobenzenesulfonic acid | HCID 66825 | — |
| Edukt | 7-Methyl-8-oxononanoic acid | HCID 22266823 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Methanol--water (1/1) | HCID 22242641 | — |
| Produkt | 6-(2,3-dimethyl-5-sulfo-3H-indol-3-yl)hexanoic acid | HCID 59855422 | — |
Reaktionsschritte
To a stirred solution of 4-hydrazinobenzenesulfonic acid (Aldrich, 11.25 g, 0.06 mol) in acetic acid (50 ml) was added 7-acetyloctanoic acid (16.7 g, 0.09 mol). The reaction mixture was heated under reflux for 12 hrs. Acetic acid was removed under reduced pressure. The resulting solid was dissolved in methanol and reprecipitated with a saturated solution of potassium hydroxide in isopropanol. The solid was filtered, washed with isopropanol and dried, (8 g, 40%). The analytical sample was obtained by C18 reversed phase column chromatography using water/methanol mixture as solvent, m.p. 250° C. dec; IR ν cm−1=2930, 2597, and 1719. 1H NMR, D2O, δ, 7.8-7.9 (m, 2H, 4-H and 6-H of aromatic protons); 7.6 (d, J=7 Hz, 1H, 7-H of aromatic); 2.2 (t, J=7 Hz, 2H, —CH2—COOH); 1.9-2.1 (m, 2H, alkyl); 1.2-1.6 (a singlet merged in a multiplet, 7H, —CH3, (—CH2)2); 0.6-0.9 (m, 2H, alkyl.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08044203B2 |
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| Quelldatensatz | uspto-grants-2011_10 |
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| ORD ID | ord-f6a651a0128f4f3b8e959c2a44e0274c |
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| Quellennotiz | uspto-grants-2011_10 |
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