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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 261749Erstellt: 24. Oktober 2026

Acetic Acid → 4-Bromo-3'-trifluoromethylacetoacetanilide

https://huagongshe.com/de/reaction/261749

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktIodineHCID 807—
EduktBromineHCID 24408—
Edukt3-oxo-N-[3-(trifluoromethyl)phenyl]butanamideHCID 744366—
LösungsmittelWaterHCID 962—
Produkt4-Bromo-3'-trifluoromethylacetoacetanilideHCID 2234769695,3%

Reaktionsschritte

A one-liter reaction flask equipped with a mechanical stirrer, air-cooled condenser, thermometer and dropping funnel was charged with 290 ml of acetic acid and 167.3 g (0.68 mole) of 3'-trifluoromethylacetoacetanilide. Only a portion of the latter dissolved. The dropping funnel contained 108.8 g (0.68 mole) of bromine, a crystal of iodine and 65 ml of acetic acid. The pot mixture was stirred as the bromine solution was added dropwise while maintaining the reaction temperature at 20°-25°. The reaction solids appeared to dissolve and reprecipitate as the bromine addition was continued. When about 65% of the bromine solution had been added, a clear reaction solution was obtained. All material remained in solution when the remaining quantity of bromine solution was added. The reaction solution was allowed to stir overnight at ambient temperature. On the following morning, the solidified mass was added to 2.8 liters of cold water and stirred. The white solid was collected on a vacuum filter and the filter cake was washed with an additional one liter of water. After drying, there was obtained 210 g (95%) of 4-bromo-3'-trifluoromethylacetoacetanilide, m.p. 66°-8°. N.M.R. (CDCl3) ##STR3##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04152329
Quelldatensatzuspto-grants-1979_05
ORD IDord-9113547183a549da8a3fca26f947ee0e
Quellennotizuspto-grants-1979_05