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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-PyridinecarboxaldehydeHCID 14273—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl diethylphosphinoacetateHCID 86596459—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product(E)-tert-Butyl 3-(pyridin-2-yl)acrylateHCID 1089975378.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399759B2
Source datasetuspto-grants-2008_07
ORD IDord-8f9f6aa6740e40b4a6b320cca86627da
Source noteuspto-grants-2008_07