Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030568Generated: November 2, 2026

Sodium Bicarbonate → HCID 15171473, compound

https://huagongshe.com/reaction/1030568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 14999123HCID 14999123—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15171473HCID 1517147391.3%

Reaction Steps

A 1M solution (15 ml) of tetrabutylammonium fluoride in tetrahydrofuran was added dropwise to a solution of 3-dimethylaminoethyl-5-(3-t-butyldimethylsilyloxypropyl)-2-(3-pyridyl)thiazolidin-4-one (2.6 g, 6.02 mmol) of dry tetrahydrofuran (12 ml) under cooling with ice. Then the mixture was stirred at room temperature for 2 hours to complete the reaction. Saturated aqueous NaHCO3 (10 ml) was added dropwise to the product mixture, and the resulting aqueous layer was extracted 6 times with ethyl acetate. The extract was dried over MgSO4, and the solvent was removed under reduced pressure. The residual crude product was purified by medium-pressure liquid chromatography (Si-60® Art. 9385, eluent : hexane : ethanol : aqueous ammonia=3000:400:50), giving 3-dimethylaminoethyl-5-(3-hydroxypropyl)-2-(3-pyridyl)thiazolidin-4-one (1.7 g, 88% yield). IR (CHCl3) [cm-1 ]; 3400 (br), 1670, 1595, 1580, 1360. NMR (CDCl3) [δ ppm]; 2.16 (6 H, s), 4.10-4.15 (1 H, m), 5.86 (1 H, d, J=2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106860
Source datasetuspto-grants-1992_04
ORD IDord-56b0f1fa63554ea8b71d2b6e9fff89ca
Source noteuspto-grants-1992_04