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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 992196생성일: 2026년 10월 23일

Nitrobenzene → 1,5-bis(Phenyl-p-tolylamino)naphthalene

https://huagongshe.com/ko/reaction/992196

반응식

참여 물질

역할이름HCID투입량
반응물NitrobenzeneHCID 7416—
반응물Potassium CarbonateHCID 11430—
반응물IodobenzeneHCID 11575—
반응물4-IodotolueneHCID 12207—
반응물1,5-DiaminonaphthaleneHCID 16720—
반응물1,5-Bis(phenylamino)naphthaleneHCID 229939—
촉매CopperHCID 23978—
용매TolueneHCID 1140—
생성물1,5-bis(Phenyl-p-tolylamino)naphthaleneHCID 18411142—

반응 조건

온도200 °C

반응 단계

8 gram (0.05 mol) of 1,5-diamino naphthalene, 22 gram (0.11 mol) of iodobenzene, 17 gram (0.12 mol) of potassium carbonate, 0.4 gram of copper powder and 50 milliliter of nitrobenzene were introduced in a 100 milliliter three-necked flask for stirring at 200° C. for 30 hours. After the reaction, toluene was added, followed by filtration for removal of inorganic compounds. Toluene and nitrobenzene were removed by distillation in a reduced pressure ambient, and the remainder was subjected to separation refinement in a silica gel column using a 1:3 mixture solvent of toluene and ligroin, to prepare 10 gram of 1,5-bis(phenylamino)naphthalene. Thereafter, 6.2 gram (0.02 mol) of 1,5-bis(phenylamino)naphthalene, 11 gram (0.05 mol) of p-iodotoluene, 7 gram (0.05 mol) of potassium carbonate, 0.3 gram of copper powder and 50 milliliter of nitrobenzene were introduced in a 100 milliliter three-necked flask for stirring at 200° C. for 30 hours. After the reaction, toluene was added, followed by filtration for removal of inorganic compounds. Toluene and nitrobenzene were removed by distillation in a reduced pressure ambient, and the remainder was subjected to separation refinement in a silica gel column using a 1:3 mixture solvent of toluene and ligroin, to prepare 7 gram of 1,5-bis(phenyl-p-tolylamino)naphthalene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06468675B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-ffdd0ddee9ae40e1a80bf09ab9ee792c
출처 메모uspto-grants-2002_10