戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 877294作成日:2026年10月26日

Diphenylamine → 4-(Diphenylamino)benz[a]anthracene

https://huagongshe.com/reaction/877294

反応式

関与物質

役割名称HCID仕込み量
反応物DiphenylamineHCID 11487—
反応物Di-tert-butylchlorophosphineHCID 139566—
反応物Benz(a)anthracene, 4-bromo-HCID 182324—
反応物Sodium t-butoxideHCID 23676156—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物4-(Diphenylamino)benz[a]anthraceneHCID 59412792—

反応条件

温度60 °C

反応手順

190 μl (1 mmol) of chlorodi-tert-butylphosphine and then 112 mg (0.5 mmol) of palladium(II) acetate are added to a suspension of 15.4 g (50 mmol) of 4-bromobenz[a]anthracene, 10.2 g (60 mmol) of diphenylamine and 7.7 g (80 mmol) of sodium tert-butoxide in 500 ml of toluene, and the mixture is subsequently heated under reflux for 5 h. After the mixture has been cooled to 60° C., 500 ml of water are added, the organic phase is separated off, filtered through silica gel, evaporated virtually to dryness at 80° C. in vacuo, and 300 ml of ethanol are then added. After cooling, the solid is filtered off with suction. Recrystallisation five times from dioxane (about 8 ml/g); sublimation (p=5×10−5 mbar, T=280° C.). Yield: 12.7 g (32 mmol), 64.1%, purity 99.9% (HPLC), Tg=74.7° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08986852B2
出典データセットuspto-grants-2015_03
ORD IDord-3d424e238af145848f7273db027f9b8e
出典メモuspto-grants-2015_03