HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912396Generated: October 30, 2026
Hydrochloric Acid → 4-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride)
https://huagongshe.com/reaction/912396
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 −60 degrees C., and added with 567 mL (884.9 mmol) of hexane solution of 1.56M n-butyllithium in drops while being stirred. Then, the reaction mixture was stirred for two hours at −60 degree C. 416 g (2.21 mol) of triisopropyl borate was dropped into the reaction solution at −60 degrees C. Subsequently, the reaction mixture was stirred for 17 hours at room temperature. The reaction mixture was further added with solution of hydrochloric acid to be stirred for one hour at room temperature. After the reaction, the reaction mixture was further added with toluene, so that aqueous phase thereof was eliminated. After organic phase thereof was dried with magnesium sulfate, 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 | US08025815B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-5669aff797644dc48cfc93f849cbb28e |
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| Source note | uspto-grants-2011_09 |
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