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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174435Generated: November 1, 2026

Potassium Carbonate → 9-Phenylanthracene

https://huagongshe.com/reaction/1174435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant9-BromoanthraceneHCID 74062—
ReactantTri-o-tolylphosphineHCID 80271—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
Solvent1,2-DimethoxyethaneHCID 8071—
Product9-PhenylanthraceneHCID 1176685%

Reaction Conditions

Temperature80 °C

Reaction Steps

5.4 g (21.1 mmol) of 9-bromoanthracene, 2.6 g (21.1 mmol) of phenylboronic acid, 60 mg (0.21 mmol) of Pd(OAc)2 (0), 10 mL (20 mmol) of an K2CO3 aqueous solution of 2M, 263 mg (0.84 mmol) of P(o-tolyl)3, and 20 mL of 1,2-dimethoxyethane (abbreviation: DME) are mixed, and then stirred for 9 hours at 80° C. 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 natural filtration, when the filtrate is condensed, 21.5 g of 9-phenylanthracene which is a target substance was obtained as a light brown solid at a yield of 85% (Synthesis Scheme (f-1)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838128B2
Source datasetuspto-grants-2010_11
ORD IDord-2a9b99bba1e147aba9bccef4f0dd8843
Source noteuspto-grants-2010_11