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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-Trimethylbenzeneboronic acidHCID 292184—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86613887HCID 86613887—
CatalystHCID 178418397HCID 178418397—
Solventtert-ButanolHCID 6386—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 67266808HCID 6726680848%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897607B2
Source datasetuspto-grants-2011_03
ORD IDord-b7cc21dd0e924abfb0083ab481dedb39
Source noteuspto-grants-2011_03