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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2,4-Trimethylbenzene | HCID 7247 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 9-Bromoanthracene | HCID 74062 | — |
| Reactant | Triphenylen-2-ylboronic acid | HCID 59805119 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-(Anthracen-9-yl)triphenylene | HCID 86701357 | 59.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09070885B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-37c36c6b3dbf46e79cb0d4a12e44d24d |
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| Source note | uspto-grants-2015_06 |
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