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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80288생성일: 2026년 10월 24일

Potassium Carbonate → 9-Phenylanthracene

https://huagongshe.com/ko/reaction/80288

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 (abbr.: Pd(OAc)2), 10 mL (20 mmol) of potassium carbonate solution (2.0 mol/L), 260 mg (0.8 mmol) of tris(o-tolyl)phosphine (abbr.: P(o-tolyl)3), and 20 mL of ethylene glycol dimethyl ether, and then the mixture was stirred at 80° C. under a nitrogen stream for 9 hours. After the stirring, 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 saline, followed by drying with magnesium sulfate. This suspending solution was gravity 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 (X-1)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08845926B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2b8e723bb9f346eb9c93e8870d62acd4
출처 메모uspto-grants-2014_09