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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 437051Erstellt: 26. Oktober 2026

Potassium Carbonate → 1-(o-Fluorobenzyl)-2[(di-sec-butylamino)acetyl]pyrrole

https://huagongshe.com/reaction/437051

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktDI-Sec-butylamineHCID 12277—
Edukt2-Chloro-1-{1-[(2-fluorophenyl)methyl]-1H-pyrrol-2-yl}ethan-1-oneHCID 20391531—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelO-XyleneHCID 7237—
Produkt1-(o-Fluorobenzyl)-2[(di-sec-butylamino)acetyl]pyrroleHCID 20391558—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 16.0 g of 2-chloroacetyl-1-(o-fluorobenzyl)pyrrole, Example 1a, 8.3 g of di-sec-butylamine and 20.0 g of potassium carbonate in 250 ml xylene is stirred at 120° C. for 72 hours. The mixture is cooled, washed with water, dried and filtered and the xylene is evaporated leaving a brown oil. The oil is dissolved in ether and extracted into a 2N hydrogen chloride solution. The aqueous acidic solution is basified with a sodium carbonate solution and extracted with ether. The ether solution is washed, dried and filtered and the ether removed leaving a brown oil of 1-(o-fluorobenzyl)-2[(di-sec-butylamino)acetyl]pyrrole. Infrared and nuclear magnetic resonance spectra confirm this structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04029672
Quelldatensatzuspto-grants-1977_06
ORD IDord-4510cb9941db4bcf8af22680c94c132b
Quellennotizuspto-grants-1977_06