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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600153Generated: October 29, 2026

Tetrahydrofuran → 9-(4-Methylphenyl)anthracene

https://huagongshe.com/reaction/600153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium CarbonateHCID 10340—
Reactant9-BromoanthraceneHCID 74062—
ReactantTolylboronic acidHCID 79799—
CatalystTolylboronic acidHCID 79799—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product9-(4-Methylphenyl)anthraceneHCID 264399107.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

5 g (1 eq, 15.6 mmol) of 9-bromo anthracene, 3.61 g of p-tolylboronic acid (1.7 eq, 26.5 mmol), 2.15 g (1.3 eq, 20.3 mmol) of Na2CO3, and 0.54 g (0.03 eq, 0.47 mmol) of tetrakis(triphenylphosphine)palladium were put into a 500-ml round-bottomed flask in Ar gas condition. 5 ml of THF and 2.2 ml of water, based on 1 mmol of p-tolylboronic acid, were added into the flask and refluxed at 85° C. for 16 hours. After the color of the solution changed to dark brown, water was added to the solution, and the organic phase was extracted using ethyl acetate. The extracted organic phase was dried using anhydrous magnesium sulfate and filtered to remove the solvent. The dried organic phase was dissolved in a small amount of toluene and separated using column chromatography (silica and hexane). A resulting solid was recrystallized using toluene and methanol to obtain 4.5 g (86%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07901793B2
Source datasetuspto-grants-2011_03
ORD IDord-86e36f830a8e4266bec3e881714b5477
Source noteuspto-grants-2011_03