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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 588369Erstellt: 25. Oktober 2026

Ethanol → ethyl 4-iodo-1-methyl-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/588369

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktOxalyl chlorideHCID 65578—
Edukt4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acidHCID 673687—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produktethyl 4-iodo-1-methyl-1H-pyrazole-5-carboxylateHCID 6013669889%

Reaktionsschritte

4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acid (301.68 g, 1.2 moles) was slurried in 1.2 L of DCM and DMF (2.3 g, 31 mmol) followed by addition of oxalyl chloride (115 mL, 1.3 moles) over 37 minutes and then stirred at room temperature for 3 h. To the resulting solution was added EtOH (750 mL, 12.9 mol) over 5 min followed by stirring at room temperature for 2 h. The crude product solution was concentrated to dryness in vacuo and then reconstituted in 1.2 L of warm heptane followed by filtration. The filtrate was concentrated by removing 500 mL of heptane, resulting in precipitation of solids. The solids were collected via filtration and dried to afford ethyl 4-iodo-1-methyl-1H-pyrazole-5-carboxylate as a white solid (297.6 g, 89% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09227956B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-884fe9457511462fa089a6eb1ba3a546
Quellennotizuspto-grants-2016_01