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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 895834생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/895834

반응식

참여 물질

역할이름HCID투입량
반응물Tetrachloro-p-hydroquinoneHCID 66603—
반응물TetrafluorophthalonitrileHCID 74600—
생성물1,4-Bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzeneHCID 11330937—

반응 단계

The objective 1,4-bis(3,4-dicarboxytrifluorophenoxy)tetrachlorobenzene dianhydride is produced as an embodiment by reacting tetrafluorophthalonitrile and tetrachlorohydroquinone (or its metal salts such as 2 Na salt; it is summarized as “tetrachlorohydroquinone”) in the presence of a base in a solvent at a temperature of −20° C. to 200° C. for 0.1 to 20 hours to form 1,4-bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene (Step 1a); hydrolyzing the resulting 1,4-bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene with an acid at a temperature of 50° C. to 300° C. for 0.5 to 20 hours to form 1,4-bis(3,4-dicarboxytrifluorophenoxy)tetrachlorobenzene (Step 1b); dissolving the reaction solution including 1,4-bis(3,4-dicarboxytrifluorophenoxy)tetrachlorobenzene in a medium containing an organic solvent once, purifying and separating the product therefrom (Step 1c); and then dehydrating the separated 1,4-bis(3,4-dicarboxytrifluorophenoxy)tetrachlorobenzene (Step 1d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06916959B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-7011c87327d6418db94653766a998e8b
출처 메모uspto-grants-2005_07