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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1708591Erstellt: 24. Oktober 2026

Dimethylformamide → Chlorfenapyr

https://huagongshe.com/de/reaction/1708591

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
EduktDiethoxymethaneHCID 10024—
EduktPhosphorus oxychlorideHCID 24813—
EduktTralopyrilHCID 183559—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
ProduktChlorfenapyrHCID 9177894,6%

Reaktionsbedingungen

Temperatur35 °C

Reaktionsschritte

A stirred mixture of 4-bromo-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carbonitrile (17.4 g, 0.05 mole), diethoxymethane (10.4 g, 0.10 mole) and dimethylformamide (DMF) (4.6 g, 0.0625 mole) in toluene, under N2, is treated portion-wise with phosphorous oxychloride (9.6 g, 0.0625 mole) at 35°-45° C. over a 10 minute period, heated at 45°-53° C. for about 0.5 hour, cooled to 35° C. and treated dropwise with triethylamine (7.25 g, 0.0715 mole) over a 2 hour period at 35°-45° C. The reaction mixture is treated with water and the toluene is removed via azeotropic distillation. The remaining residue is treated with water, filtered and the filtercake is dried in vacuo at 60° C. to give the title product, 20.8 g, 92.7% pure, 94.6% yield, identified by HPLC analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05359090
Quelldatensatzuspto-grants-1994_10
ORD IDord-06272aa97ad144cc9ba7983b6d33c56a
Quellennotizuspto-grants-1994_10