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HRID 444662作成日:2026年10月27日

Potassium Carbonate → 9-Phenylanthracene

https://huagongshe.com/reaction/444662

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 (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)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08475935B2
出典データセットuspto-grants-2013_07
ORD IDord-bd8731d07a4b4e3abd48af477f59ad25
出典メモuspto-grants-2013_07