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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493243Generated: October 31, 2026

Sodium Chloride → HCID 14649073, compound

https://huagongshe.com/reaction/1493243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 54298516HCID 54298516—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductHCID 14649073HCID 1464907312%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A n-butyllithium solution (10 ml, 16 mmol) in hexane was added to dropwise to a solution of diisopropylamine (2.84 ml, 15.9 mmol) in dry tetrahydrofuran (6 ml) at -20° to -30° 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). The resulting mixture was kept at -78° C. for 1 hour. After addition of methyl iodide (2.26 g, 15.9 mmol), this reaction mixture was slowly warmed up to the room temperature and allowed to stand overnight. The resulting 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 purified by column chromatography, giving 5,5-dimethyl-3-(2-dimethylaminoethyl)-2-(3-pyridyl)thiazolidin-4-one (257 mg, 12% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021435
Source datasetuspto-grants-1991_06
ORD IDord-69a64443265c4b4aa0e301a2fc69efb3
Source noteuspto-grants-1991_06