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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1351759생성일: 2026년 10월 27일

Tetrachloro-p-hydroquinone → 1,4-Bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene

https://huagongshe.com/reaction/1351759

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참여 물질

역할이름HCID투입량
반응물Tetrachloro-p-hydroquinoneHCID 66603—
반응물TetrafluorophthalonitrileHCID 74600—
반응물Potassium FluorideHCID 522689—
용매AcetonitrileHCID 6342—
생성물1,4-Bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzeneHCID 1133093784.4%

반응 조건

온도80 °C

반응 단계

In a 500 ml 4-necked flask, were poured 71.15 g (355 mmol) of tetrafluorophthalonitrile, 2.16 g (37.1 mmol) of potassium fluoride and 210 g of acetonitrile, and resulting was heated to 80° C. This mixture was kept at 80° C. with stirring, and to this mixture were dropped 4.40 g (17.7 mmol) of tetrachlorohydroquinone in 200 ml of acetonitrile over 1 hour. After dropping, reaction was performed at 80° C. for 6 hours. The reaction solution was cooled, filtrated, and the resulting residue washed with 30 ml and 15 ml of acetonitrile. After the filtrate had been concentrated on an evaporator to remove the solvent, 62.34 g of tetrafluorophthalonitrile was removed under in vacuo. To this was poured 27 ml of toluene and reflux performed for 1 hour. After cooling, the residue was washed with 5 ml, 25 ml and 5 ml of toluene, respectively, and further 12 ml of deionized water for three times. Finally, by drying the residue at 70° C. in vacuo, 9.08 g of 1,4-bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene were obtained (yield: 84%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07217827B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-c4b94c6ced3e49f886b5d1c0500496f8
출처 메모uspto-grants-2007_05