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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179861Generated: November 1, 2026

1,2,4-Trimethylbenzene → 2-(Anthracen-9-yl)triphenylene

https://huagongshe.com/reaction/2179861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,4-TrimethylbenzeneHCID 7247—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant9-BromoanthraceneHCID 74062—
ReactantTriphenylen-2-ylboronic acidHCID 59805119—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product2-(Anthracen-9-yl)triphenyleneHCID 8670135759.9%

Reaction Steps

Under the nitrogen atmosphere, triphenylen-2-ylboronic acid (5.6 g), 9-bromoanthracene (3.5 g), (Pd(PPh3)4) (0.5 g), potassium phosphate (5.8 g), and a mixture solvent of pseudo cumene, t-butyl alcohol, and water (48 ml) (pseudo cumene/t-butyl alcohol/water=10/1/1 (volume ratio)) were added to a flask and then refluxed for 8 hours. After adding water, the precipitates were collected by suction filtration. The obtained solid was washed with water followed by methanol and purified by silica gel column chromatography (solvent: toluene). After re-crystallization with a mixture solution of toluene/ethyl acetate, 2-(anthracen-9-yl)triphenylene (3.3 g) was obtained as an eleventh intermediate compound. The scheme is represented in the following “Reaction 21”.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09070885B2
Source datasetuspto-grants-2015_06
ORD IDord-37c36c6b3dbf46e79cb0d4a12e44d24d
Source noteuspto-grants-2015_06