HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 261748Erstellt: 26. Oktober 2026
Water → 3-oxo-N-[3-(trifluoromethyl)phenyl]butanamide
https://huagongshe.com/reaction/261748
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | O-Xylene | HCID 7237 | — |
| Edukt | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Edukt | Ethyl Acetoacetate | HCID 8868 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 3-oxo-N-[3-(trifluoromethyl)phenyl]butanamide | HCID 744366 | 55,7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04152329 |
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| Quelldatensatz | uspto-grants-1979_05 |
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| ORD ID | ord-19aa31f3ede248ceb38e78348d237a49 |
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| Quellennotiz | uspto-grants-1979_05 |
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