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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43890Erstellt: 23. Oktober 2026

Potassium Carbonate → Ethyl 3-{3-[(tert-butoxycarbonyl)amino]azetidin-1-yl}benzoate

https://huagongshe.com/de/reaction/43890

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktEthyl 3-iodobenzoateHCID 143542—
EduktL-ProlineHCID 145742—
Edukt3-Aminoazetidine, 3-BOC protectedHCID 1519405—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 3-{3-[(tert-butoxycarbonyl)amino]azetidin-1-yl}benzoateHCID 6840585057,2%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A suspension of 3-tert-butoxycarbonylaminoazetidine (300 mg, 1.74 mmol), ethyl 3-iodobenzoate (721 mg, 2.61 mmol) and copper (I) iodide (66 mg, 0.35 mmol), proline (80 mg, 0.70 mmol) and potassium carbonate (721 mg, 5.22 mmol) in DMSO was stirred at 120° C. for two hours. The reaction solution was diluted with ethyl acetate and then filtered. The filtrate was washed with brine and then dried over anhydrous magnesium sulfate. Following filtration, the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=4/1) to obtain 319 mg of the title compound as a milk white solid (57%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536197B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-5a04a1605eb34951a9345797ad1dceed
Quellennotizuspto-grants-2013_09