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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535234생성일: 2026년 10월 26일

Potassium Carbonate → 9-Phenylanthracene

https://huagongshe.com/reaction/535234

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Phenylboronic AcidHCID 66827—
반응물9-BromoanthraceneHCID 74062—
반응물Tri-o-tolylphosphineHCID 80271—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물9-PhenylanthraceneHCID 11766—

반응 단계

In a 200 mL three-neck flask, 6.4 g (25 mmol) of 9-bromoanthracene, 3.0 g (25 mmol) of phenylboronic acid, 0.76 g (2.5 mmol) of tri(ortho-tolyl)phosphine, 60 mL of ethylene glycol dimethyl ether (DME), and 25 mL 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, 0.11 g (0.50 mmol) of palladium(II) acetate was added and stirred under nitrogen stream at 80° C. for 3 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 subjected to suction filtration through Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135), and alumina, and the filtrate was condensed to give a solid. The solid was recrystallized with toluene/methonol, so that 5.8 g of target white powder was obtained in a yield of 92%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859108B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-6f04b398be644656aa03265da7b39083
출처 메모uspto-grants-2014_10