Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570328Generated: October 25, 2026

tert-Butyl acrylate → Ethyl 6-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)imidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/570328

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acrylateHCID 15458—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
ReactantBis(cyclohexylmethyl)amineHCID 4594378—
ReactantEthyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylateHCID 22031055—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 6-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)imidazo[1,2-a]pyridine-3-carboxylateHCID 78048034—

Reaction Conditions

Temperature95 °C

Reaction Steps

A stirring mixture of ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate (24s) (500 mg, 1.86 mmol), tert-butyl acrylate (408 uL, 2.79 mmol), tris(dibenzylideneacetone)diplalladium(0) (51 mg, 0.056 mmol), [(t-Bu)3PH]BF4 (27 mg, 0.093 mmol) and N,N-dicyclohexylmethylamine (738 uL, 3.48 mmol) in anhydrous 1,4-dioxane (5 mL) was heated at 95° C. overnight. The reaction was cooled to room temperature and filtered. The solvent was concentrated and the crude product was purified by silica chromatography to yield ethyl 6-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)imidazo[1,2-a]pyridine-3-carboxylate (70). MS m/z 317.14 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023839B2
Source datasetuspto-grants-2015_05
ORD IDord-1bc872b2f7dd46718a82986435eb1401
Source noteuspto-grants-2015_05