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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1713022Erstellt: 23. Oktober 2026

Potassium Carbonate → HCID 11525330, Verbindung

https://huagongshe.com/de/reaction/1713022

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2-(4-nitro-phenyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid ethyl esterHCID 59463445—
EduktHCID 86618327HCID 86618327—
EduktEthyl 4-isothiocyanato-3,3-dimethylbutanoateHCID 86618331—
LösungsmittelChloroformHCID 6212—
ProduktHCID 11525330HCID 1152533099,6%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

2-(4-nitro-phenyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid ethyl ester (212 mg, 0.71 mmol, 1 molequivalent), prepared as described hereinabove (see, preparation of Compound 1), was placed in a round bottom flask and 4-isothiocyanato-3,3-dimethyl-butyric acid ethyl ester (1.4 grams, 7.1 mmol, 10 molequivalents) was added thereto, followed by addition of grinded anhydrous potassium carbonate (K2CO3; 147 mg, 1.1 mmol, 1.5 molequivalents). The mixture was heated while stirring at 140° C. for 16 hours. The reaction mixture was thereafter dissolved in chloroform and 5% citric acid solution, the organic phase was extracted, and the aqueous layer was washed with chloroform several times. The combined organic layers were dried over Na2SO4, the solvent was removed under reduced pressure, and the crude product was triturated in ethanol to give Compound 7 (322 mg, 40% yield) as an orange solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07795255B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-bce17004c4be48ebab39dcc0564a406c
Quellennotizuspto-grants-2010_09