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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324717생성일: 2026년 10월 25일

Toluene → Bis(4-diphenylaminophenyl)amine

https://huagongshe.com/reaction/324717

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물N,N-Diphenyl-p-phenylenediamineHCID 75371—
반응물Calcium ChlorideHCID 5284359—
반응물Aluminum(III) ChlorideHCID 6451240—
용매TridecaneHCID 12388—
생성물Bis(4-diphenylaminophenyl)amineHCID 987073366.9%

반응 단계

In a 500-ml four-necked flask were charged 68 ml of tridecane (boiling point: 234° C.) as a solvent and 130.2 g (0.50 mol) of 4-diphenylaminoaniline, followed by the addition of 15.4 g (0.138 mol) of anhydrous calcium chloride and 18.5 g (0.138 mol) of anhydrous aluminum chloride under stirring. The resulting mixture was reacted at 210 to 220° C. for 3 hours under a nitrogen atmosphere. After cooling, the reaction mixture was added with 114 ml of toluene, followed by charging in 144 g of ice water. The resulting mixture was stirred and allowed to stand, and then the resulting water layer was separated out. The organic layer was washed successively with 90 ml of a 5% aqueous solution of hydrochloric acid, 60 ml of a 5% aqueous solution of sodium bicarbonate and 60 ml of water. After removal of the organic solvent by distillation under reduced pressure, 72 ml of isopropyl alcohol was added to the residue and the mixture was crystallized overnight at −3 to −8C. The resulting crude crystals were collected by filtration, washed with 27 ml of isopropyl alcohol and then dried, whereby 84.2 g (yield: 66.9%) of the title compound was obtained as pale yellow crystals. As a result of HPLC. analysis (column: YMC-A-312, detection UV: 280 nm, flow rate: 1.0 ml/min, eluent: methanol/tetrahydrofuran=99/1), the compound was found to have a purity of 99.7%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218576B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-50382a95a19b4a58a15cb176bd38f5b1
출처 메모uspto-grants-2001_04