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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871813Generated: October 29, 2026

Triethylamine → 2-(4-Bromophenyl)triphenylene

https://huagongshe.com/reaction/871813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
ReactantBenzene, 1-bromo-3-iodo-HCID 11561—
Reactant1,4-Dihydro-1,4-epoxytriphenyleneHCID 12667979—
CatalystZincHCID 23994—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
Product2-(4-Bromophenyl)triphenyleneHCID 5817485462%

Reaction Conditions

Temperature110 °C

Reaction Steps

Compound A (4.0 g, 16.4 mmol), zinc (10.72 g, 163.9 mmol), PdCl2(PPh3)2 (1.16 g, 1.7 mmol), and 1-bromo-4-iodobenzene (4.64 g, 16.4 mmol) or 1-bromo-3-iodobenzene were charged in a two-necked bottle. The bottle was then vacuumed and purged with nitrogen, and dried toluene (100 mL) and triethyl amine (23.0 mL, 165.9 mmol) were added to the bottle. The mixture in the bottle was heated to 110° C. for reaction for 24 hours, and the resulting was filtered to remove metal. The filtrate was condensed to remove the solvent, and then purified by chromatography with hexanes to obtain B (3.90 g, yield=62%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08974920B2
Source datasetuspto-grants-2015_03
ORD IDord-6174dcc545a14f29adf9fe3aa17eda30
Source noteuspto-grants-2015_03