HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429329Generated: October 30, 2026
Hydrochloric Acid → 2-(9-Phenanthrenyl)naphthalene-7-boronic acid
https://huagongshe.com/reaction/1429329
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 7-Bromo-2-(9-phenanthrenyl)naphthalene | HCID 57540015 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(9-Phenanthrenyl)naphthalene-7-boronic acid | HCID 58544628 | 85% |
Reaction Steps
In argon atmosphere, a liquid mixture of 12.27 (32.01 mmol) of 7-bromo-2-(9-phenanthrenyl)naphthalene and 130 ml of dry THF was cooled to −70° C., and 24.8 ml (38.4 mmol) of a 1.56 M hexane solution of n-butyllithium was added dropwise under stirring. Further, the reaction mixture was stirred at −70° C. for 4 h. The reaction mixture was added dropwise with 18.06 g (96.04 mmol) of triisopropyl borate while maintaining the temperature at −60° C. or lower and then stirred for one hour. The reaction mixture was heated, stirred at room temperature for 3 h, and then allowed to stand overnight. The reaction mixture was added with 100 ml of a 6 N hydrochloric acid while maintaining the temperature at 20° C. or lower by cooling on an ice bath. The reaction mixture was stirred at room temperature for 30 min, added with dichloromethane, and then allowed to separate into liquid phases. The organic phase was washed with water and dried over anhydrous sodium sulfate. The solvent was removed by distillation to obtain 9.50 g (yield: 85%) of 2-(9-phenanthrenyl)naphthalene-7-boronic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940412B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-a6c504ab49ab46a6a2271d216e185e51 |
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| Source note | uspto-grants-2015_01 |
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