HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909959Generated: October 30, 2026
Hydrochloric Acid → [3-(Naphthalen-1-yl)phenyl]boronic acid
https://huagongshe.com/reaction/909959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 3-(1-Naphthyl)-1-bromobenzene | HCID 22138047 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-(Naphthalen-1-yl)phenyl]boronic acid | HCID 58881077 | 71.9% |
Reaction Steps
Under an argon gas atmosphere, a mixture of 200.0 g (706.3 mmol) of 1(3-bromophenyl)naphthalene and 2.1 L of dehydrated THF was cooled down to −60 degrees C., and added with 543 ml (847 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. 398.5 g (2.119 mol) of triisopropyl borate was dropped into the reaction solution at −60 degrees C. Subsequently, the reaction mixture was warmed up to room temperature, and stirred for 17 hours. 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 3-(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 | US08021574B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-0f238e604f6e41a081bb9798db468472 |
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| Source note | uspto-grants-2011_09 |
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