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HRID 535236作成日:2026年10月26日

Potassium Carbonate → 2-[4-(10-Phenyl-9-anthryl)phenyl]benzoxazole

https://huagongshe.com/reaction/535236

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Tri-o-tolylphosphineHCID 80271—
反応物9-Bromo-10-phenyl-anthraceneHCID 4155836—
反応物(4-(Benzo[d]oxazol-2-yl)phenyl)boronic acidHCID 57958561—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-[4-(10-Phenyl-9-anthryl)phenyl]benzoxazoleHCID 5796732181.9%

反応手順

In a 50 mL three-neck flask, 1.0 g (3.0 mmol) of 9-bromo-10-phenylanthracene, 0.72 g (3.0 mmol) of 4-(benzoxazol-2-yl)phenylboronic acid, 0.10 g (0.32 mmol) of tri(ortho-tolyl)phosphine, 20 mL of ethylene glycol dimethyl ether (DME), and 3.0 mL (6.0 mmol) of a 2.0 M potassium carbonate solution were placed. The mixture was degassed by being stirred under reduced pressure, and the air in the flask was replaced with nitrogen. To the mixture, 14 mg (0.062 mmol) of palladium(II) acetate was added, and the mixture was stirred under nitrogen stream at 80° C. for 6 hours. After a certain period, water was added to the mixture, and an aqueous layer was extracted with toluene. The obtained extracted solution and the organic layer were combined and washed with saturated saline, and the organic layer was dried with magnesium sulfate. The mixture was gravity filtered, and the obtained filtrate was condensed to give an oily substance. The oily substance was purified by silica gel column chromatography (toluene:hexane=2:1) and recrystallized with toluene/methanol, giving 1.1 g of the target pale yellow powder in a yield of 81%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08859108B2
出典データセットuspto-grants-2014_10
ORD IDord-bbc884e4a01f4227a18865eb1ab7b307
出典メモuspto-grants-2014_10