Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57082Erstellt: 23. Oktober 2026

Tetrahydrofuran → methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate

https://huagongshe.com/de/reaction/57082

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktCeric ammonium nitrateHCID 180504—
EduktMethyl 3-chloro-1-(pyridine-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylateHCID 118022669—
LösungsmittelWaterHCID 962—
Produktmethyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylateHCID 118022666—

Reaktionsschritte

In step b of Scheme 2, methyl 3-chloro-1-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylate (6c) is oxidized with diammonium cerium (IV) nitrate (CAN) in water and polar solvents such as tetrahydrofuran at temperatures from about 0° C. to about 30° C. to yield methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate (6d). It was surprisingly discovered that the oxidation in step b can also proceed with potassium permanganate (KMnO4) as the oxidant in polar solvents such as acetone at temperatures from about 0° C. to about 30° C. However, many standard oxidation procedures such as, for example potassium persulfate (K2S2O8), iodine pentoxide (I2O5), copper oxide (CuO), and hydrogen peroxide were found to be inoperative.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434712B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-b97d2d1d8aee4941b85b5295b8212e23
Quellennotizuspto-grants-2016_09