HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1819731Erstellt: 26. Oktober 2026
Acetic Acid → Methyl 3-(4-trifluoromethylphenylamino)-2-pentenoate
https://huagongshe.com/reaction/1819731
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Toluene | HCID 1140 | — |
| Edukt | 4-(Trifluoromethyl)aniline | HCID 9964 | — |
| Edukt | Methyl 3-oxovalerate | HCID 121699 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 3-(4-trifluoromethylphenylamino)-2-pentenoate | HCID 68545758 | 72,8% |
Reaktionsschritte
In a 1 L-flask were placed 4-trifluoromethylaniline (161 g, 1.00 mol), methyl 3-oxopentanoate (130 g, 1.00 mol) and toluene (160 mL). To this solution was added acetic acid (16 g, 0.27 mol), and the resulting mixture was heated in a bath kept at 100° C. under a reduced pressure of 19 kPa for 3.5 hours, while the water generated was taken out of the reaction system by using a Dean-Stark trap under reflux. Acetic acid (16 g, 0.27 mol) was then added, and reflux was continued for 4.5 hours. Acetic acid (8 g, 0.13 mol) was then added again, and reflux was continued for another 2.5 hours. The heating was then discontinued, nitrogen leaked in, and the reaction mixture cooled. After distillation of the solvent and acetic acid under reduced pressure, the residue was distilled under reduced pressure to give 199 g of the title compound. The yield was 72.8%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07601842B2 |
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| Quelldatensatz | uspto-grants-2009_10 |
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| ORD ID | ord-a5b7a54b457948e4a9b314aabba51ac7 |
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| Quellennotiz | uspto-grants-2009_10 |
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