HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184198Generated: October 26, 2026
Water → ethyl 3-[(1E)-4-methoxybut-1-en-1-yl]imidazo[1,2-a]pyridine-2-carboxylate
https://huagongshe.com/reaction/1184198
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl 3-formylimidazo[1,2-a]pyridine-2-carboxylate | HCID 10704014 | — |
| Reactant | (3-Methoxypropyl)triphenylphosphonium bromide | HCID 21458797 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 3-[(1E)-4-methoxybut-1-en-1-yl]imidazo[1,2-a]pyridine-2-carboxylate | HCID 58355141 | 12% |
Reaction Steps
To a suspension of (3-methoxypropyl)(triphenyl)phosphonium bromide (3.56 g) in THF (50 ml) was added potassium tert-butoxide (0.38 g) at −78° C., and the mixture was stirred at the same temperature for 30 min. Ethyl 3-formylimidazo[1,2-a]pyridine-2-carboxylate (1.7 g) was added to the reaction mixture, and the mixture was stirred at room temperature for 12 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate was concentrated under reduced pressure to give the object product (256 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08664380B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-4aa351816e814496835ee3e4430ea003 |
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| Source note | uspto-grants-2014_03 |
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