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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030563Generated: November 2, 2026

Sodium Chloride → HCID 14999119, compound

https://huagongshe.com/reaction/1030563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantIodoethaneHCID 6340—
ReactantDiisopropylamineHCID 7912—
ReactantHCID 54298516HCID 54298516—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 14999119HCID 1499911983%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium solution (5 ml, 8 mmol) in hexane was added dropwise to a solution of diisopropylamine (1.42 ml, 7.96 mmol) in dry tetrahydrofuran at -30° to -40° C. The mixture was kept between those temperatures for 1 hour and then cooled to -78° C. Thereto was added dropwise a solution of 3-(2-dimethylaminoethyl)-2-(3-pyridyl)thiazolidin-4-one (2 g, 7.96 mmol) in dry tetrahydrofuran (10 ml). This reaction mixture was kept at that temperature for 1 hour. Then, ethyl iodide (1.24 g, 7.96 mmol) was added, and this reaction mixture was slowly warmed up to room temperature and maintained there for 30 minutes. The resulting mixture, after addition of aqueous NaCl, was extracted with ethyl acetate. The extract was washed with aqueous NaCl, dried, and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography, giving 5-ethyl-3-(2-dimethylaminoethyl)-2-(3-pyridyl)thiazolidin-4-one (1.84 g, 83% yield). NMR (CDCl, δ) [ppm]; 1.06 (3 H, t, J=7.3 Hz), 2.15 (6 H, s), 3.75-3.85 (1 H, m), 4.00-4.05 (1 H, m), 5.86 (1 H, d, J=2.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106860
Source datasetuspto-grants-1992_04
ORD IDord-5cdb64f0f670429eaafbe65820f16126
Source noteuspto-grants-1992_04