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HRID 80288作成日:2026年10月23日

Potassium Carbonate → 9-Phenylanthracene

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

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%

反応手順

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)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08845926B2
出典データセットuspto-grants-2014_09
ORD IDord-2b8e723bb9f346eb9c93e8870d62acd4
出典メモuspto-grants-2014_09