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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221183Generated: October 30, 2026

Methanol → HCID 16122314, compound

https://huagongshe.com/reaction/221183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3,3′′-Dimethoxy-1,1′:2′,1′′-terphenylHCID 16122220—
CatalystIron chloride (FeCl3)HCID 24380—
SolventDichloromethaneHCID 6344—
ProductHCID 16122314HCID 1612231470.5%

Reaction Steps

Into a flask, 2 g of 1,2-bis(3-methoxyphenyl)benzene was put, and allowed to dissolve in 100 ml of dichloromethane under nitrogen atmosphere. In the solution, 3.25 g of iron(III) chloride was added, and the solution was stirred at room temperature for 56.5 hours. Methanol was added to terminate the reaction, and then the solution was washed by water. The organic layer was purified by silica gel column chromatography, and then recrystallized in a toluene/heptane mixed solvent, and thus 1.4 g of 2,7-dimethoxytriphenylene was obtained. Obtained 2,7-dimethoxytriphenylene was converted to 2,7-dihydroxytriphenylene by boron tribromide, and allowed to react with trifluoromethanesulfonyl chloride, and converted to 2,7-bis(trifluoromethanesulfonyloxy)triphenylene. The product was allowed react with bis(pinacolate)diboron, and thus 2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolanyl)triphenylene was synthesized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202633B2
Source datasetuspto-grants-2012_06
ORD IDord-5b78d75bb38548288b051798ac288750
Source noteuspto-grants-2012_06