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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914421Generated: October 29, 2026

Dimethylformamide → HCID 86101308, compound

https://huagongshe.com/reaction/1914421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBromobenzeneHCID 7961—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 86629340HCID 86629340—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
ProductHCID 86101308HCID 86101308—

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixed solution of 0.61 g of 2-[1-(4-t-butylphenyl)pyren-7-yl]-4,4,5,5-tetramethyl 1,3,2-dioxaborolane, 0.28 mL of bromobenzene, 1.2 g of tripotassium phosphate, 0.18 g of tetrabutylammonium bromide, 14 mg of palladium acetate and 15 mL of dimethylformamide was heated and stirred under a nitrogen gas stream at 130° C. for 8 hours. The solution was cooled to room temperature and poured into 75 mL of water, and then the precipitated solid was collected by filtration. The resulting solid was dissolved in dichloromethane, washed with water, dried over magnesium sulfate and then concentrated. The resulting crude product was purified by column chromatography and then vacuum-dried to obtain 0.49 g of 1-(4-t-butylphenyl)-7-phenylpyrene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08610345B2
Source datasetuspto-grants-2013_12
ORD IDord-42d16eec4fd94a7db2b6b3de8a4deeff
Source noteuspto-grants-2013_12