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HRID 1289346Erstellt: 25. Oktober 2026

Dimethylformamide → 3-(2,5-Dimethyl-5-hexene-3-oxy)phthalonitrile

https://huagongshe.com/reaction/1289346

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium hydrideHCID 24758—
Edukt2,5-Dimethyl-5-hexen-3-olHCID 144264—
Edukt1,2-Benzenedicarbonitrile, 3-nitro-HCID 162652—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt3-(2,5-Dimethyl-5-hexene-3-oxy)phthalonitrileHCID 1892102586%

Reaktionsschritte

9.6 g (0.24 mol) of 60% sodium hydride and 150 ml of N,N-dimethylformamide were placed in a container equipped with a stirrer, a reflux condenser and a nitrogen-introducing tube, and the solution was then stirred under the feed of nitrogen. Afterward, 32 g (0.25 mol) of 2,5-dimethyl-5-hexene-3-ol was added dropwise thereto at 20°-30° C. over 1 hour, and the solution was then stirred at the same temperature for 3 hours to prepare a sodium alcoholate solution. Next, 34.6 g (0.2 mol) of 3-nitrophthalonitrile and 150 ml of N,N-dimethylformamide were placed in a container equipped with a stirrer, and the above-mentioned sodium alcoholate solution was then added dropwise at 0° C. or less over 5 hours. After completion of the addition, the temperature of the solution was raised up to a level of 20°-30° C., and the solution was then stirred for 2 hours to bring reaction to an end. The thus obtained reaction solution was poured into 3 l of water and then stirred for 30 minutes, and 500 ml of toluene were added. After stirring for 30 minutes, the solution was allowed to stand to separate a toluene layer. After toluene was distilled off under reduced pressure, recrystallization was carried out from 500 ml of n-hexane to obtain 43.7 g of 3-(2,5-dimethyl-5-hexene-3-oxy)phthalonitrile (yield =86.0%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05750229
Quelldatensatzuspto-grants-1998_05
ORD IDord-ee0c4eff8678454d9eb4eb5ad607ce67
Quellennotizuspto-grants-1998_05