Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1354011Erstellt: 25. Oktober 2026

Ethanesulfonyl chloride → 8-(Ethylsulfonylamino)octanoic acid

https://huagongshe.com/reaction/1354011

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanesulfonyl chlorideHCID 11667—
Edukt8-Aminooctanoic acidHCID 66085—
LösungsmittelSodium HydroxideHCID 14798—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt8-(Ethylsulfonylamino)octanoic acidHCID 2110322938%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07223745B2
Quelldatensatzuspto-grants-2007_05
ORD IDord-872bfeb0b0ba49698f5da157e4508b9c
Quellennotizuspto-grants-2007_05