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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2292655Erstellt: 26. Oktober 2026

Potassium Carbonate → 2-[2-Chloro-4-(1-pyrazolyl)methylphenoxy]ethylcarbamic acid methyl ester

https://huagongshe.com/reaction/2292655

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktAmmonium ChlorideHCID 25517—
EduktMethyl (2-chloroethyl)carbamateHCID 251614—
Edukt2-chloro-4-(2-2H-1,2,3-triazolylmethyl)phenolHCID 21833677—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-[2-Chloro-4-(1-pyrazolyl)methylphenoxy]ethylcarbamic acid methyl esterHCID 5714985574,2%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a mixture of potassium carbonate (435 mg), 2-chloro-4-(2-2H-1,2,3-tri-azolyl)methylphenol (300 mg) and anhydrous N,N-dimethylformamide (30 ml) was added dropwise an anhydrous N,N-dimethylformamide solution (2 ml) of 2-chloroethylcarbamic acid methyl ester (216 mg) at room temperature under stirring. This mixture was then heated at 60° C. under stirring for 6 hours, and poured into ice-cooled saturated aqueous ammonium chloride solution, which was extracted with ethyl acetate. The organic layer was washed with water and then saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, which afforded 329 mg of 2-[2-chloro-4-(1-pyrazolyl)methylphenoxy]ethylcarbamic acid methyl ester (compound 7). Yield, 74%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05684022
Quelldatensatzuspto-grants-1997_11
ORD IDord-7fb194e164834ab09957857f7bedc501
Quellennotizuspto-grants-1997_11