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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 261748Erstellt: 26. Oktober 2026

Water → 3-oxo-N-[3-(trifluoromethyl)phenyl]butanamide

https://huagongshe.com/reaction/261748

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktO-XyleneHCID 7237—
Edukt3-(Trifluoromethyl)anilineHCID 7375—
EduktEthyl AcetoacetateHCID 8868—
LösungsmittelHexaneHCID 8058—
Produkt3-oxo-N-[3-(trifluoromethyl)phenyl]butanamideHCID 74436655,7%

Reaktionsschritte

A two-liter reaction flask fitted with a magnetic stirrer, heating mantle, dropping funnel, thermometer, water-cooled condenser and Dean Stark trap was charged with 156.2 g (1.2 moles) of ethyl acetoacetate and 400 ml of xylene. The dropping funnel contained 161 g (1.0 mole) of 3-aminobenzotrifluoride and 320 ml xylene. The solution in the reaction pot was heated to 135° and the contents of the dropping funnel were added dropwise over a period of three hours. The low-boiling liquid which accumulated in the Dean Stark trap was periodically drained in order to maintain a reaction temperature of about 135°. After four hours, the reaction was judged to be completed and the reaction solution was cooled. There was added 650 ml of hexane. Cooling in an ice bath yielded a white crystalline precipitate. The product was collected on a vacuum filter and dried in an oven. There was obtained 136.6 g (55.7%) of 3'-trifluoromethylacetoacetanilide, m.p. 109°-10°. N.M.R. (CDCl3) ∂ 2.2 (CH3, keto), 3.5 (CH2), 7.2-7.9 (aromatic), 1.8 (CH3, enol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04152329
Quelldatensatzuspto-grants-1979_05
ORD IDord-19aa31f3ede248ceb38e78348d237a49
Quellennotizuspto-grants-1979_05