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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5391Erstellt: 23. Oktober 2026

Iodine → cis Ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/de/reaction/5391

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktBromineHCID 24408—
EduktPhosphorus pentachlorideHCID 24819—
EduktEthyl 2-oxo-1-azacyclodecane-10-carboxylateHCID 19930826—
LösungsmittelDichloromethaneHCID 6344—
Produktcis Ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylateHCID 131718120—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Ethyl 2-oxo-1-azacyclodecane-10-carboxylate (4.0 g, 17.6 mmol) is dissolved in methylene chloride (50 mL), and cooled to 0° C. Phosphorus pentachloride (3.85 g, 18.5 mmol) and iodine (0.051 g, 0.2 mmol) are added. The reaction is stirred for 15 minutes at 0° C. Then, bromine (3.10 g, 19.4 mmol) is added, and the reaction is stirred at 0° C. for 4 hours. The reaction is quenched by adding saturated sodium sulfite (until the color of excess bromine disappears), and extracted several times with methylene chloride. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (15% ethyl acetate/hexane) to give cis ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate, m.p. 132°-134° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244889
Quelldatensatzuspto-grants-1993_09
ORD IDord-506b9adb631a461cb9ffccba8d2f7bb0
Quellennotizuspto-grants-1993_09