HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514006Generated: November 3, 2026
Hexane → (6-Phenylnaphthalen-2-yl)boronic acid
https://huagongshe.com/reaction/1514006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 2-Bromo-6-phenylnaphthalene | HCID 15311215 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (6-Phenylnaphthalen-2-yl)boronic acid | HCID 57539613 | 87.6% |
Reaction Steps
In an atmosphere of argon, 360 g (1.27 mol) of 2-bromo-6-phenylnaphthalene, 2 L of dehydrated diethyl ether and 2 L of dehydrated toluene were charged and cooled to −10° C. Then, 1 L (1.58 mol) of a hexane solution of 1.58M n-butyl lithium was added dropwise, and stirred at −10° C. for 5 hours. The reaction solution was cooled to −60° C., and after adding 718 g (3.81 mol) of triisopropyl borate, the mixture was stirred at room temperature for 17 hours. After adding 1 L of toluene and 1 L of water, the resulting mixture was stirred for an hour. Then, an aqueous layer was removed. An organic layer was washed with water, and dried with magnesium sulfate. The organic layer was concentrated, and heat-washed with toluene, whereby 276 g of 6-phenylnaphthalene-2-boronic acid was obtained (yield: 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08221907B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-2549a37f851d4cf98f5c8c97e59222d7 |
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| Source note | uspto-grants-2012_07 |
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