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
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Reactant | Bis(cyclohexylmethyl)amine | HCID 4594378 | — |
| Reactant | Ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate | HCID 22031055 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 6-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)imidazo[1,2-a]pyridine-3-carboxylate | HCID 78048034 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023839B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-1bc872b2f7dd46718a82986435eb1401 |
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| Source note | uspto-grants-2015_05 |
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