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HRID 634535作成日:2026年10月26日

Aniline → N,N,N'-triphenyl-4-phenylenediamine

https://huagongshe.com/reaction/634535

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物HexaneHCID 8058—
反応物Tris(1,1-dimethylethyl)phosphineHCID 83681—
反応物4-BromotriphenylamineHCID 642838—
反応物Sodium t-butoxideHCID 23676156—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
溶媒TolueneHCID 1140—
生成物N,N,N'-triphenyl-4-phenylenediamineHCID 16128842%

反応条件

温度80 °C

反応手順

0.56 g (6 mmol) of 4-bromotriphenylamine, 0.35 g (0.6 mmol) of bis(dibenzylideneacetone)palladium(0), and 0.58 g (6 mmol) of sodium-tert-butoxide were put into a 100 mL three neck flask, and 5 mL of toluene was added thereto. After nitrogen was substituted for the content of the flask, 0.56 g (6 mmol) of aniline and 0.37 mL (1.8 mmol) of a hexane solution (10 wt %) of tri-tert-butylphosphine were added. This mixture was stirred for 5 hours at 80° C. to be reacted. After the reaction, the reaction was completed by adding a saturated saline solution to the reaction mixture, and an aqueous layer was extracted by approximately 100 mL of ethyl acetate to be separated from an organic layer. The organic layer was dried with magnesium sulfate and filtered. A solid that was obtained by concentrating the filtrate was purified by silica column chromatography, whereby 0.24 g of a light yellow powder solid of DPA that is an object was obtained in the yield of 42% (Synthesis Scheme (i-2)). For the column purification, a mixed solvent of ethyl acetate:hexane=1:20 was used as a developing solvent.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09324951B2
出典データセットuspto-grants-2016_04
ORD IDord-1691873a788845f5b96f46aaca1dabf3
出典メモuspto-grants-2016_04