HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2217924Erstellt: 27. Oktober 2026
4-Fluoro-3-nitrobenzoic acid → 4-Fluoro-3-nitro-N,N-bis(2,2,2-trifluoroethyl)benzamide
https://huagongshe.com/reaction/2217924
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Fluoro-3-nitrobenzoic acid | HCID 67987 | — |
| Edukt | Bis(2,2,2-trifluoroethyl)amine | HCID 78999 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | DCM thionyl chloride | HCID 21879677 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-Fluoro-3-nitro-N,N-bis(2,2,2-trifluoroethyl)benzamide | HCID 58911744 | — |
Reaktionsschritte
4-Fluoro-3-nitrobenzoic acid (2.50 g, 13.5 mmol) was refluxed in a 2:1 mixture of CH2Cl2/SOCl2 (150 mL) for 5 h. The solvent was concentrated and the residue was dissolved in CH2Cl2 (50 mL). Another CH2Cl2 solution (50 mL) of diisopropylethylamine (DIPEA) (3.50 mL, 20.3 mmol) and bis(2,2,2-trifluoroethyl)amine (4.90 g, 27.0 mmoL) was then added dropwise to the cold stirring solution (0° C.) of the acid chloride. The solution was stirred at RT overnight. The solution was then washed with 5% KHSO4 solution, saturated NaHCO3 solution, and brine and dried over anhydrous MgSO4. The product was purified by flash chromatography on silica gel using 3:1/HEX:EtOAc. Yield: 3.08 g (66%); 1H NMR (CDCl3) 4.17 (brs, 4H), 7.40 (t, J=8.59 Hz, 1H), 7.66 (m, 2H), 8.10 (d, J=6.84 Hz, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07407968B2 |
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| Quelldatensatz | uspto-grants-2008_08 |
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| ORD ID | ord-16dffafa98fe4a68ad9da965631bb6c9 |
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| Quellennotiz | uspto-grants-2008_08 |
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