HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289309Generated: October 31, 2026
Triisopropyl borate → (5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid
https://huagongshe.com/reaction/1289309
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 6-Bromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene | HCID 10586063 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid | HCID 22571498 | — |
Reaction Steps
To a cold (-78° C.) solution of 2.02 g (8.4 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene in 11.0 mL of toluene, was added 4.6 g (6.8 mL, 10.9 mmol, 1.6M in hexane) of n-BuLi. The resulting solution was stirred at -78° C. for 45 min. and then 2.40 g (3.0 mL, 12.7 mmol) of triisopropylborate was dropwise added and the reaction stirred at room temperature for 12 h. The reaction was then diluted with 10% HCl, and extracted with ether (2 x). The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Recrystallization from hexane afforded the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747542 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-e1ec370d0a684745a94eba6d8640f4a3 |
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| Source note | uspto-grants-1998_05 |
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