HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748147Generated: October 29, 2026
Water → (E)-tert-Butyl 3-(pyridin-2-yl)acrylate
https://huagongshe.com/reaction/748147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Tert-butyl diethylphosphinoacetate | HCID 86596459 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (E)-tert-Butyl 3-(pyridin-2-yl)acrylate | HCID 10899753 | 78.6% |
Reaction Steps
Sodium hydride (60% oil, 0.6 g, 15.7 mmol) was washed with hexane and suspended in tetrahydrofuran (5 ml). To the mixture, a solution of tert-butyl diethylphosphinoacetate (2.5 g, 9.8 mmol) in tetrahydrofuran (2 ml) was added under ice cooling condition. The reaction mixture was stirred at room temperature for 30 minutes, cooled under ice cooling condition. A solution of 2-formylpyridine (1.0 g, 9.3 mmol) in tetrahydrofuran (3.0 ml) was added to the mixture, and the mixture was stirred at 0° C. for 1.5 hrs. The reaction mixture was combined with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to a silica gel (60 g) column chromatography, and eluted with hexane-ethyl acetate (3:1, v/v) to give the titled compound (1.5 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399759B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-8f9f6aa6740e40b4a6b320cca86627da |
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| Source note | uspto-grants-2008_07 |
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