Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241995Erstellt: 23. Oktober 2026

Triethylamine → Ethyl 2-diazo-3-(2-fluorophenyl)-3-oxopropanoate

https://huagongshe.com/de/reaction/241995

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl 3-(2-fluorophenyl)-3-oxopropanoateHCID 296342—
Edukt4-Acetamidobenzenesulfonyl azideHCID 5129185—
LösungsmittelAcetonitrileHCID 6342—
ProduktEthyl 2-diazo-3-(2-fluorophenyl)-3-oxopropanoateHCID 76818128—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Ethyl 3-(2-fluorophenyl)-3-oxopropanoate (1.00 g, 4.76 mmol) was dissolved in acetonitrile (14 mL) and treated with triethylamine (0.760 ml, 5.47 mmol, 1.15 equiv). The mixture was cooled to 0° C., treated with 4-acetamidobenzenesulfonylazide (1.26 g, 5.23 mmol, 1.1 equiv) and warmed to ambient temperature over 1.5 hours. The mixture was partially concentrated in vacuo, cooled to 0° C., treated with sodium hydroxide (50 mL, 1 N aqueous) and extracted with chloroform (3×50 mL). The combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified via silica gel gradient chromatography (100:0 to 85:15; hexanes:ethyl acetate) providing the titled compound as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653079B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-6ab024c191ed49abb57df564e3e0ab5e
Quellennotizuspto-grants-2014_02