HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183932Generated: November 1, 2026
Potassium Acetate → 2,4-Difluoro-3-(pyridin-3-yl)benzeneboronic acid
https://huagongshe.com/reaction/2183932
Participants
| Role | Name | HCID | Charge |
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| 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 1M 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 2,4-difluoro-3-(pyridin-3-yl)benzeneboronic acid (2.2 g, 85%) as a grey solid: m/z (ES+) 236 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900215B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-55487be94dd14405850fedc9b86e69d3 |
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| Source note | uspto-grants-2005_05 |
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