HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045299Generated: October 30, 2026
Hydrochloric Acid → 4-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride)
https://huagongshe.com/reaction/1045299
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-(4-bromophenyl)naphthalene | HCID 11208338 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride) | HCID 44119399 | 68.9% |
Reaction Steps
Under an argon gas atmosphere, a mixture of 208.8 g (737.4 mmol) of 1-(4-bromophenyl)naphthalene and 2.1 L of dehydrated THF was cooled down to minus 60 degree C. Then, 567 ml (884.9 mmol) of hexane solution of 1.56M n-butyllithium was dropped into the mixture while the mixture was being stirred. The reaction mixture was further stirred at minus 60 degrees for 2 hours. 416 g (2.21 mol) of triisopropylborate was dropped into the reaction mixture at minus 60 degrees C. The reaction mixture was then stirred at room temperature for 17 hours. The reaction mixture was added with aqueous solution of hydrochloric acid and stirred at room temperature for 1 hour. After the reaction, the reaction mixture was added with toluene, and aqueous phase thereof was eliminated. Then, organic phase thereof was dried with magnesium sulfate, and the solvent was distilled away under reduced pressure. By recrystallizing the obtained solid by toluene, 126 g of 4-(1-naphthyl)phenylboronic acid was obtained at an yield of 67%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08568903B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-7ba21a6bd01f4f52814d5dca8b509f0c |
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| Source note | uspto-grants-2013_10 |
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