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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030557Generated: November 3, 2026

Sodium Chloride → HCID 14999093, compound

https://huagongshe.com/reaction/1030557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14999088HCID 14999088—
SolventDimethylformamideHCID 6228—
ProductHCID 14999093HCID 1499909355%

Reaction Steps

5-Methyl-2-(3-pyridyl)thiazolidin-4-one (10 g, 51.5 mmol) and ethyl bromoacetate (6.85 ml, 61.8 mmol) were dissolved in dry dimethylformamide (50 ml), and 60% sodium hydride (2.16 g, 54.1 mmol) was added in limited amounts to the solution at 0° to 10° C. This reaction mixture was kept between those temperatures for 1 hour. The mixture, after addition of aqueous NaCl, was extracted with ethyl acetate. The extract was washed with aqueous NaCl, dried, and the solvent was removed in vacuo. The residue was chromatographed on silica gel, giving the cis-isomer (5.8 g) (compound No. 9) and the trans-isomer (2.1 g) (compound No. 10) of the title compound (55% yield). Compound No. 9: cis-isomer NMR (CDCl3, δ) [ppm]; 1.24 (3 H, t, J=7.2 Hz), 1.67 (3 H, d, J=7.1 Hz), 5.81 (1 H, s). IR (CHCl3) [cm-1 ]; 2950, 1740, 1683, 1587, 1575, 1441, 1370, 1014. Compound No. 10: trans-isomer NMR (CDCl3, δ) [ppm]; 1.25 (3 H, t, J=7.2 Hz), 1.68 (3 H, d, J=7.1 Hz), 5.83 (1 H, d, J=1.7 Hz). IR (CHCl3) [cm-1 ]; 2950, 1739, 1685, 1585, 1572, 1370, 1345, 1012.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106860
Source datasetuspto-grants-1992_04
ORD IDord-555170571f334f72b27f4b66f9735225
Source noteuspto-grants-1992_04