HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720549Generated: October 29, 2026
Triisopropyl borate → 2-Fluorophenylboronic acid
https://huagongshe.com/reaction/720549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-Bromo-2-fluorobenzene | HCID 61259 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Fluorophenylboronic acid | HCID 2734354 | 63.1% |
Reaction Steps
A solution of 50 g (285.6 mmol) of 2-fluorobromobenzene in 400 mL of tetrahydrofuran was cooled to −78° C. and 200 mL (320.0 mmol) of 1.6M n-Butyllithium was added via a cannula. The mixture was stirred at −78° C. for 60 minutes, then 98.9 mL (428.4 mmol) of triisopropyl borate was added via a cannula and stirring was continued for 60 minutes. The cooling bath was removed and the mixture was stirred at ambient temperature for 1.5 hours, then 150 mL of 6N hydrochloric acid was added and stirring was continued for 1.5 hours. To the mixture was added 100 mL of brine, and then the organic layer was separated and the aqueous layer was extracted three times with 30 mL each of ether. The combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo. The residue was recrystallized from water to afford 25.2 g (63%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135487B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-139002d775564f46a4568ef5d85a054e |
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| Source note | uspto-grants-2006_11 |
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