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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410278Generated: October 25, 2026

Ethyl 2-pyridinecarboxylate → 1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-3-(pyridin-2-yl)propane-1,3-dione

https://huagongshe.com/reaction/1410278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-pyridinecarboxylateHCID 17307—
ReactantSodium hydrideHCID 24758—
Reactant1,4-Benzodioxan-6-yl methyl ketoneHCID 76143—
SolventTetrahydrofuranHCID 8028—
Product1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-3-(pyridin-2-yl)propane-1,3-dioneHCID 5684038471%

Reaction Steps

A solution of 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethanone (XV) (1 eq) in THF was added slowly to a suspension of NaH (1.5 eq) in THF stirred under nitrogen at room temperature. The solution was further allowed to stir at room temperature until the evolution of gas was ceased. Ethyl picolinate (XIX) (1.1 eq) was added to the solution and refluxed overnight under nitrogen. The solution was cooled, poured into ice water and extracted with ethyl acetate. The organic layer was dried over MgSO4, filtered and concentrated under vacuum. The crude product was purified by column chromatography over silica gel to produce 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-(pyridin-2-yl)propane-1,3-dione 15 as a yellow solid (71% yield), 1H NMR (CDCl3, 400 MHz): δ ppm 4.13-4.43 (m, 4H), 6.94 (d, J=8.31 Hz, 1H), 7.42 (m, 1H), 7.44 (m, 1H) 7.59 (m, 2H), 7.85 (m, 1H), 8.14 (d, J=7.81, 1H), 8.65 (m, 1H); ESIMS found C16H13NO4 m/z 284 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921413B2
Source datasetuspto-grants-2014_12
ORD IDord-2e4aa01661f74d32b74adec2069e9cda
Source noteuspto-grants-2014_12