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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 654134Erstellt: 24. Oktober 2026

Sodium ethoxide → Chlorfenapyr

https://huagongshe.com/de/reaction/654134

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ethoxideHCID 2723922—
Edukt4-Bromo-1-(chloromethyl)-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carbonitrileHCID 19888616—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktChlorfenapyrHCID 9177885,9%

Reaktionsschritte

A solution of 4-bromo-1-(chloromethyl)-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carbonitrile (2.0 g, 0.005 mol) in absolute ethanol is treated with a 21% wt/wt ethanolic solution of sodium ethoxide (0.36 g, 0.0053 mol), heated to 75°-80° C. for 20-30 minutes, cooled to room temperature and diluted with water and ether. The organic phase is dried over anhydrous magnesium sulfate and concentrated in vacuo to give a solid which is recrystallized form heptane to give the title product as a white solid (1.75 g, mp 97°-98° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05130328
Quelldatensatzuspto-grants-1992_07
ORD IDord-d87701a3380848998d4943e36ed4b71b
Quellennotizuspto-grants-1992_07