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HRID 879925作成日:2026年10月26日

Nitrogen → 2-[4-(10-Phenanthren-3-ylanthracen-9-yl)phenyl]-1-phenyl-1h-benzimidazole

https://huagongshe.com/reaction/879925

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物TolueneHCID 1140—
反応物Sodium CarbonateHCID 10340—
反応物4-(1-Phenyl-1H-benzimidazol-2-yl)phenylboronic AcidHCID 53249779—
反応物9-Bromo-10-phenanthren-3-ylanthraceneHCID 59629544—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒Methanol--water (1/1)HCID 22242641—
生成物2-[4-(10-Phenanthren-3-ylanthracen-9-yl)phenyl]-1-phenyl-1h-benzimidazoleHCID 5962957968%

反応手順

32 g (70 mmol) of 9-bromo-10-phenanthren-3-ylanthracene, 26.3 g (84 mmol) of 4-(1-phenyl-1H-benzimidazol-2-yl)phenylboronic acid and 125 ml of 2 M Na2CO3 solution are suspended in 500 ml of toluene and 500 ml of EtOH, the mixture is saturated with N2, 1.7 g (1.8 mmol) of tetrakis(triphenylphosphine)palladium(0) are added, and the mixture is heated at the boil for 2 h. The mixture is poured into 1.5 l of a mixture of water/MeOH/6 M HCl 1:1:1, and the yellow precipitate is filtered off with suction, washed with water, EtOH and toluene and dried. Subsequent Soxhlet extraction with chloroform, removal of the solvent, recrystallisation three times from toluene and sublimation twice in vacuo (p=1×10−5 mbar, T=385° C.) give 30 g (68%) of a pale-yellow powder having a purity of >99.9% (HPLC).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993123B2
出典データセットuspto-grants-2015_03
ORD IDord-ab83d728c9b84a7caab39f2bdb2bb0db
出典メモuspto-grants-2015_03