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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 537591생성일: 2026년 10월 24일

Potassium Carbonate → 9-Phenylanthracene

https://huagongshe.com/ko/reaction/537591

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 조건

온도80 °C

반응 단계

5.4 g (21.1 mmol) of 9-bromoanthracene, 2.6 g (21.1 mmol) of phenylboronic acid, 60 mg (0.21 mmol) of palladium(II) acetate (abbreviation: Pd(OAc)2), 10 mL (20 mmol) of a potassium carbonate aqueous solution (2 mol/L), 263 mg (0.84 mmol) of tris(ortho-tolyl)phosphine (abbreviation: P(o-tolyl)3), and 20 mL of 1,2-dimethoxyethane (abbreviation: DME) were put in a 200 mL three neck flask, and then stirred for nine hours at 80° C. in nitrogen stream. After reaction, a precipitated solid was collected by suction filtration. Subsequently, the solid was dissolved in toluene and then filtered through florisil, celite, and alumina. After a filtrate was washed with water and saturated saline, it was dried with magnesium sulfate. After the mixture was subjected to natural filtration, when the filtrate was concentrated, 21.5 g of 9-phenylanthracene which was a target substance was obtained as a light brown solid at a yield of 85% (Synthesis scheme (b-1)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08860019B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-4e389874e59f47cf8a297b6f7d703899
출처 메모uspto-grants-2014_10