HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598109Generated: October 25, 2026
2,4,6-Trimethylbenzeneboronic acid → 1-(6-Mesitylpyridin-2-yl)pentan-2-ol
https://huagongshe.com/reaction/598109
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trimethylbenzeneboronic acid | HCID 292184 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 6-Bromo-alpha-propyl-2-pyridineethanol | HCID 86613889 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1-(6-Mesitylpyridin-2-yl)pentan-2-ol | HCID 67267089 | 77.8% |
Reaction Steps
1-(6-Bromopyridin-2-yl)pentan-2-ol (3.23 g, 13.2 mmol) was dissolved in 30 mL of 1,2-dimethoxyethane. Tetrakis(triphenylphosphine)palladium(0) (0.76 g, 0.66 mmol) was added and the solution was heated to 50° C. for 15 min. After cooling the solution, 2,4,6-trimethylbenzeneboronic acid (2.60 g, 15.9 mmol) in 15 mL 1,2-dimethoxyethane was added to parent solution. Potassium t-butoxide (2.96 g, 26.5 mmol) in 15 mL t-butanol was added last. The reaction was heated at 90° C. for 0.5 h. After cooling, the solution was filtered and concentrated. Flash chromatography (20% ethyl acetate/hexanes) gave the title compound (2.91 g, 77% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897607B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-5d6f6713b4d14f439713ab545a3ff287 |
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| Source note | uspto-grants-2011_03 |
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