HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891861Generated: October 30, 2026
Potassium Acetate → 2,4-Difluoro-3-(pyridin-3-yl)benzeneboronic acid
https://huagongshe.com/reaction/891861
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(neopentyl glycolato)diboron | HCID 2734316 | — |
| Reactant | 3-(3-Bromo-2,6-difluorophenyl)pyridine | HCID 22240086 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2,4-Difluoro-3-(pyridin-3-yl)benzeneboronic acid | HCID 22240096 | 85.1% |
Reaction Steps
A mixture of 3-(3-bromo-2,6-difluorophenyl)pyridine (2.97 g, 11 mmol), potassium acetate (2.16 g, 22 mmol) and bis(neopentyl glycolato)diboron (2.86 g, 12.7 mmol) in 1,4-dioxane (30 ml) was heated at 90° C. for 16 h. The reaction was cooled, filtered (washing the filter cake with a small quantity of diethyl ether) and the filtrate concentrated in vacuo. The residue was partitioned between diethyl ether (100 ml) and 1 M sodium hydroxide (100 ml) and the organics discarded. The aqueous was washed with more diethyl ether and then cooled in an ice-water bath. The pH was adjusted to approximately 6 with 36% hydrochloric acid, and allowed to stand for 1 h. The resulting solid was collected by filtration and dried under vacuum to afford 2.2 g (85%) of the title compound as a grey solid: MS (ES+) m/z 236 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005431B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-cf6005a469e64472aad429d8abc5b9b9 |
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| Source note | uspto-grants-2006_02 |
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