Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173321Generated: October 26, 2026

Sodium hydride → tert-Butyl ethyl (5-nitropyridin-2-yl)malonate

https://huagongshe.com/reaction/2173321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-5-nitropyridineHCID 78308—
Reactanttert-Butyl ethyl malonateHCID 96345—
SolventDimethylformamideHCID 6228—
Producttert-Butyl ethyl (5-nitropyridin-2-yl)malonateHCID 54383765—

Reaction Steps

To a suspension of NaH (60% in oil, 1.89 g, 47 mmol) in 20 mL of DMF was added tert-butyl ethyl propanedioate (6.5 g, 34.7 mmol) at room temperature. The mixture was stirred for 30 min. A solution of 2-chloro-5-nitropyridine (5.0 g, 31.5 mmol) in 10 mL of DMF was added. The mixture was stirred at r.t. overnight. The solvent was removed under reduce pressure. Water was added and the mixture was extracted with EtOAc. The combined organic layer was washed with brine, dried over anhydrous Na2SO4, concentrated and the residue was purified by column chromatography with silca gel to give tert-butyl ethyl (5-nitropyridin-2-yl)propanedioate. 1H-NMR (400 MHz, CDCl3) δ 9.39 (s, 1H), 8.51 (d, J=8.8 Hz, 1H), 7.76 (d, J=8.8 Hz, 1H), 5.00 (s, 1H), 4.28 (q, J=7.2 Hz, 2H), 1.49 (s, 9H), 1.31 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-5098ffdd206f4a5a89ad99c2f7d443e7
Source noteuspto-grants-2015_06