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HRID 264711作成日:2026年10月27日

Dimethylformamide → 3-(3,5-Dimethyl-1,6-heptadiene-4-oxy)phthalonitrile

https://huagongshe.com/reaction/264711

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物1,2-Benzenedicarbonitrile, 3-nitro-HCID 162652—
反応物3,5-Dimethyl-1,6-heptadien-4-olHCID 537207—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物3-(3,5-Dimethyl-1,6-heptadiene-4-oxy)phthalonitrileHCID 1892116484%

反応手順

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, 35 g (0.25 mol) of 3,5-dimethyl-1,6-heptadiene-4-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 added dropwise thereto 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 3 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 resulting toluene layer was separated. After toluene was distilled off under reduced pressure, recrystallization was carried out from 600 ml of n-hexane to obtain 44.7 g of 3-(3,5-dimethyl-1,6-heptadiene-4-oxy)phthalonitrile (yield=84.0%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646273
出典データセットuspto-grants-1997_07
ORD IDord-0d152d0574234ff7a4b734d63f1742e0
出典メモuspto-grants-1997_07