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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535238생성일: 2026년 10월 25일

Toluene → 3-(Anthracen-9-yl)pyridine

https://huagongshe.com/reaction/535238

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Sodium CarbonateHCID 10340—
반응물3-BromopyridineHCID 12286—
반응물9-Anthraceneboronic AcidHCID 15510213—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물3-(Anthracen-9-yl)pyridineHCID 264388—

반응 단계

In a 200 mL three-neck flask, 5.2 g (23 mmol) of 9-anthrylboronic acid, 4.0 g (25 mmol) of 3-bromopyridine, 5.2 g (50 mmol) of sodium carbonate, 50 mL of toluene, 25 μL of ethanol, and 25 mL of water 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, 0.28 g (0.25 mmol) of tetrakis(triphenylphosphine)palladium(0) was added, and the mixture was stirred under nitrogen stream at 80° C. for 7 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, washed with saturated saline, and dried with magnesium sulfate. The obtained mixture was gravity filtered, and the filtrate was condensed to give an oily substance. The oily substance was recrystallized with toluene/hexane, so that 2.8 g of target yellow powder was obtained in a yield of 46%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859108B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-dd4688f4826642aca41ac290afdcfd0a
출처 메모uspto-grants-2014_10