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HRID 537591作成日:2026年10月25日

Potassium Carbonate → 9-Phenylanthracene

https://huagongshe.com/reaction/537591

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Phenylboronic AcidHCID 66827—
反応物9-BromoanthraceneHCID 74062—
反応物Tri-o-tolylphosphineHCID 80271—
触媒palladium(II) acetateHCID 167845—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物9-PhenylanthraceneHCID 1176685%

反応条件

温度80 °C

反応手順

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)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08860019B2
出典データセットuspto-grants-2014_10
ORD IDord-4e389874e59f47cf8a297b6f7d703899
出典メモuspto-grants-2014_10