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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50462생성일: 2026년 10월 26일

Toluene → N,N'-dianisyl-1,4-phenylenediamine

https://huagongshe.com/reaction/50462

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물4-BromoanisoleHCID 7730—
반응물P-PhenylenediamineHCID 7814—
반응물HexaneHCID 8058—
반응물Sodium t-butoxideHCID 23676156—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물N,N'-dianisyl-1,4-phenylenediamineHCID 2130160672%

반응 조건

온도90 °C

반응 단계

A flame-dried one liter three neck round bottom flask was charged with 4-bromoanisole (50.4 g, 0.26 mole), 1,4-phenylenediamine (12.0 g, 0.11 mole), 1,1 ′-bis(diphenylphosphino)ferrocene (1.776 g, 0.0032 mole), tris(dibenzylideneacetone)dipalladium(0) (0.98 g, 0.001 mole), sodium tert-butoxide (31.2 g, 0.32 mole), and anhydrous toluene (350 ml). The reaction mixture was heated to 90° C. for 48 hours. The reaction mixture was cooled to room temperature and hexane (400 ml) was added. The solid was filtered and dissolved in ethanol (400 ml). Sodium dithionite (20.0 g) was dissolved in 300 ml water and added to the ethanol solution. This was heated to reflux for 30 minutes. After the solution was cooled to room temperature, the solid was filtered off and washed with water to give 25.7 g (72%) of N,N′-dianisyl-1,4-phenylenediamine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710906B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-361d3f1358d749a78e0447ed25911790
출처 메모uspto-grants-2004_03