HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 543571Erstellt: 24. Oktober 2026
Dicyclohexylcarbodiimide → N-(3-trifluoromethyl-4-difluoromethoxyphenyl)-1-methylcyclopropanecarboxamide
https://huagongshe.com/de/reaction/543571
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | 1-Methylcyclopropanecarboxylic acid | HCID 81326 | — |
| Edukt | 4-(Difluoromethoxy)-3-(trifluoromethyl)aniline | HCID 20460099 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-(3-trifluoromethyl-4-difluoromethoxyphenyl)-1-methylcyclopropanecarboxamide | HCID 13314710 | 81,6% |
Reaktionsschritte
To a solution of 1-methylcyclopropanecarboxylic acid (1.0 g) in tetrahydrofuran (50 ml), 3-trifluoromethyl-4-difluoromethoxyaniline (2.25 g) was added, and a solution of N,N'-dicyclohexylcarbodiimide (DCC) (2.2 g) in tetrahydrofuran was dropwise added while stirring. After several minutes, the by-produced N,N'-dicyclohexylurea (DCU) was eliminated by filtration. To the filtrate, acetic acid (2 ml) was added to decompose excessive DCC, followed by elimination of DCU. The resultant filtrate was extracted with ether, and the extract was washed with 1 N hydrochloric acid, sodium hydrogen carbonate solution and saturated sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated. The crude crystals (2.85 g) were recrystallized from ethanol to give N-(3-trifluoromethyl-4-difluoromethoxyphenyl)-1-methylcyclopropanecarboxamide (2.5 g). M.P., 39°-40° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04447260 |
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| Quelldatensatz | uspto-grants-1984_05 |
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| ORD ID | ord-8e274d3e04cd48cb8713b6a544f0a839 |
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| Quellennotiz | uspto-grants-1984_05 |
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