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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535236생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/535236

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tri-o-tolylphosphineHCID 80271—
반응물9-Bromo-10-phenyl-anthraceneHCID 4155836—
반응물(4-(Benzo[d]oxazol-2-yl)phenyl)boronic acidHCID 57958561—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-[4-(10-Phenyl-9-anthryl)phenyl]benzoxazoleHCID 5796732181.9%

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859108B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-bbc884e4a01f4227a18865eb1ab7b307
출처 메모uspto-grants-2014_10