HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600153Generated: October 29, 2026
Tetrahydrofuran → 9-(4-Methylphenyl)anthracene
https://huagongshe.com/reaction/600153
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 9-Bromoanthracene | HCID 74062 | — |
| Reactant | Tolylboronic acid | HCID 79799 | — |
| Catalyst | Tolylboronic acid | HCID 79799 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 9-(4-Methylphenyl)anthracene | HCID 264399 | 107.5% |
Reaction Steps
5 g (1 eq, 15.6 mmol) of 9-bromo anthracene, 3.61 g of p-tolylboronic acid (1.7 eq, 26.5 mmol), 2.15 g (1.3 eq, 20.3 mmol) of Na2CO3, and 0.54 g (0.03 eq, 0.47 mmol) of tetrakis(triphenylphosphine)palladium were put into a 500-ml round-bottomed flask in Ar gas condition. 5 ml of THF and 2.2 ml of water, based on 1 mmol of p-tolylboronic acid, were added into the flask and refluxed at 85° C. for 16 hours. After the color of the solution changed to dark brown, water was added to the solution, and the organic phase was extracted using ethyl acetate. The extracted organic phase was dried using anhydrous magnesium sulfate and filtered to remove the solvent. The dried organic phase was dissolved in a small amount of toluene and separated using column chromatography (silica and hexane). A resulting solid was recrystallized using toluene and methanol to obtain 4.5 g (86%) of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07901793B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-86e36f830a8e4266bec3e881714b5477 |
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| Source note | uspto-grants-2011_03 |
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