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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410754Generated: October 31, 2026

Lithium iodide → 3-(Ethoxycarbonyl)-1-benzyl-1,2-dihydro-2-oxopyridine-4-carboxylic acid

https://huagongshe.com/reaction/1410754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium iodideHCID 66321—
Reactant1-Benzyl-2-oxo-1,2-dihydro-pyridine-3,4-dicarboxylic acid 3-ethyl ester 4-methyl esterHCID 68297279—
SolventPyridineHCID 1049—
Product3-(Ethoxycarbonyl)-1-benzyl-1,2-dihydro-2-oxopyridine-4-carboxylic acidHCID 6829737946%

Reaction Steps

A solution of 1-benzyl-2-oxo-1,2-dihydro-pyridine-3,4-dicarboxylic acid 3-ethyl ester 4-methyl ester (4.1 g, 13 mmol) in 10 mL of pyridine was added to a refluxing mixture of LiI (7.0 g, 52 mmol) and 50 mL of pyridine. The resulting mixture was refluxed for 1 h. After the mixture was cooled to r.t., solvent was evaporated in vacuo. The residue was taken up in water (150 mL) and acidified to pH about 2 with 6M HCl. The resulting suspension was extracted several times with CHCl3, and the organic layers were combined and dried over MgSO4. After solvent was evaporated in vacuo, the crude product was chromatographed (100% EtOAc) to give 1.8 g of the title compound as a yellow solid. 1H NMR (CDCl3, 200 MHz): δ=7.20-7.45 (m, 6H), 6.61 (d, 1H, J=7.0 Hz), 5.16 (s, 2H), 4.41 (q, 2H, J=7.4 Hz), 1.37 (t, 3H, J=6.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921389B2
Source datasetuspto-grants-2014_12
ORD IDord-ce5109e8c0e24b239160a8c3e0e0c534
Source noteuspto-grants-2014_12