HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906831Generated: October 30, 2026
Triisopropyl borate → (6-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid
https://huagongshe.com/reaction/906831
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 5-Bromo-2-ethoxy-3-(trifluoromethyl)pyridine | HCID 67389975 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (6-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid | HCID 67389387 | 78.6% |
Reaction Steps
Alternatively, n-butyl lithium (1.6 M solution in hexane, 0.9 mL, 1.43 mmol) was slowly added to a solution of 5-bromo-2-ethoxy-3-trifluoromethyl-pyridine (352 mg, 1.3 mmol) in 2.6 mL anhydrous Et2O at −78° C. under nitrogen. The mixture was kept at −78° C. for 1 hr, and then to this mixture was added triisopropyl borate (489 mg, 2.6 mmol). The mixture was allowed to warm to ambient temperature overnight. The reaction was quenched by water and the pH was adjusted to 5 by carefully addition of 1N aqueous HCl. Two layers were separated and the aqueous layer was extracted with ethyl acetate three times. The extract was washed with brine, dried over sodium sulfate, and concentrated in vacuo to give 2-ethoxy-3-trifluoromethylpyridine-5-boronic acid as a brown oil (240 mg, 67% yield). The product was used for the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08013001B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-69c985d4c4834cda9958efe2d5ac9a5a |
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| Source note | uspto-grants-2011_09 |
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