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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1289347생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1289347

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물1,2-Benzenedicarbonitrile, 3-nitro-HCID 162652—
반응물3,5-Dimethyl-1,6-heptadien-4-olHCID 537207—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물3-(3,5-Dimethyl-1,6-heptadiene-4-oxy)phthalonitrileHCID 1892116484%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05750229
출처 데이터셋uspto-grants-1998_05
ORD IDord-476d5542b56448aa954832774b934bc9
출처 메모uspto-grants-1998_05