HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1350095Erstellt: 25. Oktober 2026
2,4,6-Trifluoroaniline → N-Benzyl-2-(2,4,6-trifluoro-phenylamino)-acetamide
https://huagongshe.com/reaction/1350095
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,4,6-Trifluoroaniline | HCID 67765 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | N-Benzyl-2-chloroacetamide | HCID 96233 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | N-Benzyl-2-(2,4,6-trifluoro-phenylamino)-acetamide | HCID 17954375 | 23,7% |
Reaktionsschritte
A mixture of N-benzyl-2-chloroacetamide (700 mg—obtained as described for intermediate 1), DIPEA (0.76 mL) and 2,4,6-trifluoro-aniline (559 mg) in anhydrous DMF (5 mL) was stirred at 100° C. for 40 hours under a Nitrogen atmosphere. Then, more DIPEA (0.2 mL) was added and the mixture was heated to 100° C. for further 4 hours. After cooling to room temperature, the solution was diluted with AcOEt and washed with water and ice. The separated aqueous phase was extracted with further AcOEt (3×30 mL). The combined organic extracts were dried and concentrated in vacuo. The residue was purified by flash chromatography (CH/AcOEt from 8:2 to 6:4) to give the title compound (265 mg) as a beige solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07214680B2 |
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| Quelldatensatz | uspto-grants-2007_05 |
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| ORD ID | ord-626c79338a9e48f8986e663a161a5007 |
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| Quellennotiz | uspto-grants-2007_05 |
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