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HRID 1976846Erstellt: 26. Oktober 2026

Dinitrofluorobenzene → 4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecyloxy)-1,3-dinitrobenzene

https://huagongshe.com/reaction/1976846

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDinitrofluorobenzeneHCID 6264—
EduktTriethylamineHCID 8471—
EduktDimethylacetamideHCID 31374—
Edukt1,1,2,2-Tetrahydroperfluoro-1-decanolHCID 69619—
LösungsmittelWaterHCID 962—
Produkt4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecyloxy)-1,3-dinitrobenzeneHCID 2199922072%

Reaktionsschritte

In a flask were charged 1-fluoro-2,4-dinitrobenzene (40.94 g, 0.22 mol), triethylamine (24.29 g, 0.24 mol), 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl alcohol (102.1 g, 0.22 mol), 220 g of N,N-dimethylacetamide and stirred at room temperature for 22 hours under a nitrogen atmosphere. The resultant etherified product was introduced into water with stirring. The solids precipitated were collected and dried at 40° C. under reduced pressure to obtain 97.22 g (yield: 72%) of 4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyloxy)-1,3-dinitrobenzene as yellow crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06228972B1
Quelldatensatzuspto-grants-2001_05
ORD IDord-e944ad6e126d443d92bbef3fc27b561d
Quellennotizuspto-grants-2001_05