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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 444662생성일: 2026년 10월 27일

Potassium Carbonate → 9-Phenylanthracene

https://huagongshe.com/reaction/444662

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Phenylboronic AcidHCID 66827—
반응물9-BromoanthraceneHCID 74062—
반응물Tri-o-tolylphosphineHCID 80271—
촉매palladium(II) acetateHCID 167845—
용매1,2-DimethoxyethaneHCID 8071—
생성물9-PhenylanthraceneHCID 1176685%

반응 단계

Into a 200 mL three-neck flask were put 5.4 g (21 mmol) of 9-bromoanthracene, 2.6 g (21 mmol) of phenylboronic acid, 60 mg (0.2 mmol) of palladium(II) acetate (abbreviation: Pd(OAc)2), 10 mL (20 mmol) of potassium carbonate aqueous solution (2.0 mol/L), 260 mg (0.8 mmol) of tris(o-tolyl)phosphine (abbreviation: P(o-tolyl)3), and 20 mL of 1,2-dimethoxyethane (abbreviation: DME), and then the mixture was stirred at 80° C. in a nitrogen atmosphere for 9 hours. After the reaction, a precipitated solid was collected by suction filtration, dissolved in toluene, and filtered through Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135), celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), and alumina. The obtained filtrate was washed with water and saturated aqueous solution and magnesium sulfate was added so that the moisture was removed. This suspending solution was naturally filtered and the obtained filtrate was concentrated, whereby 22 g of a light-brown solid of 9-phenylanthracene, which was the object of the synthesis, was obtained in a yield of 85% (synthesis scheme (a-1)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08475935B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-bd8731d07a4b4e3abd48af477f59ad25
출처 메모uspto-grants-2013_07