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HRID 50462作成日:2026年10月27日

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

https://huagongshe.com/reaction/50462

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物4-BromoanisoleHCID 7730—
反応物P-PhenylenediamineHCID 7814—
反応物HexaneHCID 8058—
反応物Sodium t-butoxideHCID 23676156—
触媒Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
生成物N,N'-dianisyl-1,4-phenylenediamineHCID 2130160672%

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710906B2
出典データセットuspto-grants-2004_03
ORD IDord-361d3f1358d749a78e0447ed25911790
出典メモuspto-grants-2004_03