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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt1-Methylcyclopropanecarboxylic acidHCID 81326—
Edukt4-(Difluoromethoxy)-3-(trifluoromethyl)anilineHCID 20460099—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(3-trifluoromethyl-4-difluoromethoxyphenyl)-1-methylcyclopropanecarboxamideHCID 1331471081,6%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04447260
Quelldatensatzuspto-grants-1984_05
ORD IDord-8e274d3e04cd48cb8713b6a544f0a839
Quellennotizuspto-grants-1984_05