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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420667Generated: October 31, 2026

Butyl Acrylate → Butyl (2E)-3-[2-[(2,2-dimethylpropanoyl)amino]-6-(methyloxy)-3-pyridinyl]-2-propenoate

https://huagongshe.com/reaction/420667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl AcrylateHCID 8846—
Reactantalpha-CyclohexylcyclohexanemethanamineHCID 10774245—
ReactantN-[3-Bromo-6-(methyloxy)-2-pyridinyl]-2,2-dimethylpropanamideHCID 58001713—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystHCID 178418851HCID 178418851—
SolventDichloromethaneHCID 6344—
ProductButyl (2E)-3-[2-[(2,2-dimethylpropanoyl)amino]-6-(methyloxy)-3-pyridinyl]-2-propenoateHCID 5800172995.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-[3-bromo-6-(methyloxy)-2-pyridinyl]-2,2-dimethylpropanamide (78.738 g, 274 mmol), bis(tri-t-butylphosphine)palladium(0) (1 g, 1.957 mmol) and tris(dibenzylideneacetone)dipalladium(0) (0.892 g, 0.974 mmol) in dry, degassed 1,4-dioxane (600 ml) was treated with n-butyl acrylate (47.1 ml, 329 mmol) and dicyclohexylmethylamine (64.5 ml, 302 mmol). The reaction mixture was then heated at 80° C. for 4 h and then at 120° C. for 3 h. The reaction was then evaporated and water (1000 ml) was added and the mixture was extracted with Et2O (3×500 ml). The combined organic solvents were then dried (MgSO4), filtered, evaporated to give the crude product. This was then dissolved in DCM (300 ml) and chromatographed (10-30% EtOAc:40-60 petroleum ether) and then dried in vacuo to give product as a white solid (87.412 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097628B2
Source datasetuspto-grants-2012_01
ORD IDord-c07d22eb7aa64a06bd41634d70c0ff55
Source noteuspto-grants-2012_01