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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5404Erstellt: 24. Oktober 2026

Triethylamine → 10-(Acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane

https://huagongshe.com/de/reaction/5404

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-Thiopheneacetic acidHCID 15970—
Edukt2-Fluoro-1-methylpyridinium p-toluenesulfonateHCID 171631—
Edukt3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecaneHCID 19930843—
LösungsmittelAcetoneHCID 180—
LösungsmittelBenzeneHCID 241—
Produkt10-(Acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecaneHCID 19930829—

Reaktionsschritte

3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane (0.50 g, 1.67 mmol) is dissolved in acetone (5.0 mL) and benzene (5.0 mL). Triethylamine (0.26 mL, 1.9 mmol) is added, followed by 2-fluoro-1-methylpyridinium toluene-4-sulfonate (0.54 g, 1.9 mmol), and the reaction is stirred at room temperature for 90 minutes. Thiolacetic acid (0.14 mL, 1.9 mmol) and more triethylamine (0.26 mL, 1.9 mmol) are added, and the reaction is heated to reflux for 2 hours. The solvent is then removed, the crude product is partitioned between methylene chloride and water, and the aqueous phase is extracted several times with methylene chloride. The combined organic layers are dried (MgSO4) and the solvent is evaporated. The crude product is purified by silica gel chromatography (15% ethyl acetate/hexane) to give 10-(acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane, MS: M+1=358.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244889
Quelldatensatzuspto-grants-1993_09
ORD IDord-b0cbfac023104194ba68e11d16883fb1
Quellennotizuspto-grants-1993_09