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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419677Generated: October 30, 2026

Ethyl Propionate → (S)-2-(2-Oxo-2H-pyrid-1-yl)-propionic acid ethyl ester

https://huagongshe.com/reaction/419677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl PropionateHCID 7749—
Reactant2-PyridoneHCID 8871—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-(2-Oxo-2H-pyrid-1-yl)-propionic acid ethyl esterHCID 6665004546.7%

Reaction Steps

A stirred solution of 1H-Pyridin-2-one (500 mg, 5.26 mmol) in anhydrous THF (50 ml) at room temperature was treated portionwise with 60% NaH (231 mg, 5.78 mmol). The reaction mixture was kept for 10 min then added over 5 min to a solution of (R)-2-trifluoromethanesulfonyloxy)-propionic acid ethyl ester (1315 mg, 5.26 mmol) in anhydrous THF (2.5 ml) at room temperature. The resulting mixture was stirred for 2 h, then concentrated. The residue was dissolved in ethyl acetate, and the resulting solution was washed with ice cold dilute HCl. The organic layer was removed and the aqueous layer re-extracted with ethyl acetate. The combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was purified by flash chromatography (20% up to 80% ethyl acetate in hexane) to afford the title compound as a yellow oil (480 mg, 46%): [α]27D=−56.4° (c=0.275, CH2Cl2); 1H NMR (400 MHz CDCl3) δ 1.3 (3H, t), 1.65 (3H, d), 4.2 (2H, q), 5.6 (1H, q), 6.2 (1H, t), 6.4 (1H, d), 7.2-7.3 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093392B2
Source datasetuspto-grants-2012_01
ORD IDord-87ea1f978f2f4ad4a40d731ca6927273
Source noteuspto-grants-2012_01