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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131633Erstellt: 25. Oktober 2026

Chlorodiphenylmethane → 1-(Diphenylmethyl)-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/131633

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorodiphenylmethaneHCID 7035—
EduktPotassium CarbonateHCID 11430—
Eduktethyl 1H-pyrazole-4-carboxylateHCID 142179—
LösungsmittelWaterHCID 962—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt1-(Diphenylmethyl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 69313438—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A suspension of 1H-pyrazole-4-carboxylic acid ethyl ester (1.0 g), benzhydryl chloride (1.9 ml) and potassium carbonate (1.48 g) in anhydrous 1-methyl-2-pyrrolidinone (10 ml) was heated at 100° C. under nitrogen for 6 h. It was diluted with water and extracted with ethyl acetate, the organic extracts washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with i-hexane/ethyl acetate (4:1) followed by i-hexane/ethyl acetate (2:1) to give the sub-title compound (2.18 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384951B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-b9eb24beb22d458e8dd7dc49124f29a9
Quellennotizuspto-grants-2008_06