HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1354011Erstellt: 25. Oktober 2026
Ethanesulfonyl chloride → 8-(Ethylsulfonylamino)octanoic acid
https://huagongshe.com/reaction/1354011
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethanesulfonyl chloride | HCID 11667 | — |
| Edukt | 8-Aminooctanoic acid | HCID 66085 | — |
| Lösungsmittel | Sodium Hydroxide | HCID 14798 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 8-(Ethylsulfonylamino)octanoic acid | HCID 21103229 | 38% |
Reaktionsschritte
A solution of ethanesulfonyl chloride (1.5 ml, 15.7 mmol) in dioxane (5 ml) was added to a solution of 8-aminooctanoic acid (1 g, 6.28 mmol) in 1N NaOH (22 ml) and dioxane (5 ml), while stirring at 0–5° C. The mixture was allowed to warm to room temperature and stirred for 3.5 minutes. During this period, at 1 hour intervals, the pH was adjusted to 7–8 by addition of 25% NaOH solution. The reaction mixture was washed with diethyl ether (30 ml). The pH was adjusted to 1–2 by addition of 1N HCl and the mixture was extracted with ethyl acetate (70 ml). The organic layer was dried over sodium sulfate and concentrated. The residue was triturated with a mixture of diethyl ether. The solid was collected by filtration and dried under vacuum affording 600 mg of the title compound (38% yield). 1H NMR (DMSO-d6): 11.9 (1H, s); 6.96 (1H, t, J=6 Hz); 2.96 (2H, q, J=7.1); 2.88 (2H, q, J=6.6); 2.2 (2H, t, J=7.3); 1.45 (4H, m); 1.26 (6H, m); 1.18 (3H, t, J=7.3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07223745B2 |
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| Quelldatensatz | uspto-grants-2007_05 |
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| ORD ID | ord-872bfeb0b0ba49698f5da157e4508b9c |
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| Quellennotiz | uspto-grants-2007_05 |
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