HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598096Generated: October 31, 2026
2,4,6-Trimethylbenzeneboronic acid → HCID 67266808, compound
https://huagongshe.com/reaction/598096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trimethylbenzeneboronic acid | HCID 292184 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86613887 | HCID 86613887 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 67266808 | HCID 67266808 | 48% |
Reaction Steps
N-[(6-Bromopyridin-2-yl)methyl]-N-propylpropan-1-amine (7.0 g, 26 mmol) was dissolved in 1,2-dimethoxyethane (100 mL). Tetrakis(triphenylphosphine)palladium(0) (1.49 g, 1.29 mmol) was added and the solution was heated to 50° C. for 15 minutes. The solution was cooled and 2,4,6-trimethylbenzeneboronic acid (4.44 g, 27.1 mmol) in 30 mL 1,2 dimethoxyethane was added followed by potassium tert-butoxide (5.79 g, 51.6 mmol) in 30 mL of tBuOH. The reaction was heated at 90° C. for 0.5 h. The solution was filtered through filter paper and concentrated. Flash chromatography gave 3.83 g of the title compound (48% 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-b7cc21dd0e924abfb0083ab481dedb39 |
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| Source note | uspto-grants-2011_03 |
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