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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530183Generated: October 29, 2026

Toluene → 1,6-Diphenylpyrene

https://huagongshe.com/reaction/530183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantPyrene, 1,6-Dibromo-HCID 176470—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product1,6-DiphenylpyreneHCID 59133403—

Reaction Steps

Under an argon atmosphere, 15.0 g of 1,6-dibromopyrene, 13.2 g of phenylboronic acid, 1.9 g of tetrakis(triphenylphosphine)palladium (0) [Pd(PPh3)4], 27.8 g of sodium carbonate (130 mL of clean water), toluene and tetrahydrofuran were placed into a flask, and the resulting mixture was allowed to react at 90° C. for 7 hours. After cooling, the reaction solution was filtered, and solids obtained were washed with methanol and clean water. Further, the solids were purified by silica gel chromatography (heated toluene). The resulting crude product which was obtained by a concentration was re-crystallized from toluene, followed by drying under a reduced pressure, whereby white solids of 1,6-diphenylpyrene (11.8 g) were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353027B2
Source datasetuspto-grants-2016_05
ORD IDord-67f7b26c2ed24c3ebedb3ecc71d7e8b7
Source noteuspto-grants-2016_05