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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030558Generated: November 2, 2026

Sodium Chloride → HCID 14999101, compound

https://huagongshe.com/reaction/1030558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14999089HCID 14999089—
SolventDimethylformamideHCID 6228—
ProductHCID 14999101HCID 1499910148.1%

Reaction Steps

Methyl iodide (0.72 g, 5.0 mmol) was added to a solution of 3-(2-hydroxyethyl)-5-methyl-2-(3-pyridyl)-thiazolidin-4-one (1 g, 4.2 mmol) in dry dimethylformamide (5 ml), and 40% sodium hydride (176 mg, 4.4 mmol) was added in limited amounts of the mixture under cooling with ice. Then, cooling with ice was continued for 1 hour. The product mixture was poured into aqueous NaCl, and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous Na2SO4, and filtered. The filtrate was concentrated and subjected to medium-pressure chromatography (hexane-acetone), giving 3-(2-methoxyethyl)-5-methyl-2-(3-pyridyl)-thiazolidin-4-one (0.51 g, 48% yield). NMR (CDCl3) δ [ppm]; 1.62 (0.75 H, d, J=7.1 Hz), 1.66 (2.5 H, d, J=7.1 Hz), 3.28 (2.25 H, s), 3.3 (0.75 H, s), 5.85 (1 H, s) IR (CHCl3) [cm-1 ]; 2935, 1670, 1589, 1576, 1445, 1408, 1300, 1113.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106860
Source datasetuspto-grants-1992_04
ORD IDord-0b31f91dd5174581bcd265e77f65e0c6
Source noteuspto-grants-1992_04