돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602218생성일: 2026년 10월 25일

Dodecane → N4,N4-di([1,1'-biphenyl]-4-yl)-N4'-phenyl-[1,1'-biphenyl]-4,4'-diamine

https://huagongshe.com/reaction/602218

반응식

참여 물질

역할이름HCID투입량
반응물DodecaneHCID 8182—
반응물Potassium CarbonateHCID 11430—
반응물Potassium HydroxideHCID 14797—
반응물Bis-biphenyl-4-yl-amineHCID 504244—
반응물N-(4'-iodobiphenylyl)acetanilideHCID 23140821—
촉매CopperHCID 23978—
용매WaterHCID 962—
용매Isoamyl AlcoholHCID 31260—
생성물N4,N4-di([1,1'-biphenyl]-4-yl)-N4'-phenyl-[1,1'-biphenyl]-4,4'-diamineHCID 2314081969.9%

반응 단계

There were mixed 20.70 g (0.050 mole) of N-(4′-iodobiphenylyl)acetanilide, 19.95 g (0.060 mole) of N,N-bis(biphenyl-4-yl)amine, 10.40 g (0.075 mole) of anhydrous potassium carbonate, 0.20 g (0.003 mole) of copper powder and 10 ml of n-dodecane, followed by reaction at 200 to 212° C. for 15 hours. The reaction product was extracted with 200 ml of toluene, and the insoluble matter was removed by filtration. Then, the filtrate was concentrated to obtain crude crystals. The crude crystals were dissolved in 80 ml of isoamyl alcohol, and 5 ml of water and 5.00 g (0.075 mole) of 85% potassium hydroxide were added, followed by hydrolysis at 130° C. After isoamyl alcohol was removed by steam distillation, extraction with 250 ml of toluene was performed, and the organic layer was washed with water, dried and concentrated. The concentrate was purified by column chromatography (carrier: silica gel, eluate: toluene/n-hexane=1/2) to obtain 24.2 g (yield: 69.9%, HPLC purity: 98.0%) of N,N-bis(biphenyl-4-yl)-N′-phenyl-4,4′-diaminobiphenyl. The melting point was 145.8 to 146.0° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902402B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-f943f6dd476e4a3b85ec9a000b7290d7
출처 메모uspto-grants-2011_03