HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871813Generated: October 29, 2026
Triethylamine → 2-(4-Bromophenyl)triphenylene
https://huagongshe.com/reaction/871813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-4-iodobenzene | HCID 11522 | — |
| Reactant | Benzene, 1-bromo-3-iodo- | HCID 11561 | — |
| Reactant | 1,4-Dihydro-1,4-epoxytriphenylene | HCID 12667979 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Bromophenyl)triphenylene | HCID 58174854 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08974920B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-6174dcc545a14f29adf9fe3aa17eda30 |
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| Source note | uspto-grants-2015_03 |
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