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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493249Generated: November 1, 2026

Phosphate → HCID 14999090, compound

https://huagongshe.com/reaction/1493249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantSodium IodideHCID 5238—
ReactantDiisopropylamineHCID 7912—
ReactantButyl bromideHCID 8002—
ReactantHCID 14999087HCID 14999087—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 14999090HCID 1499909020%

Reaction Steps

Dry diisopropylamine (1 ml, 5.7 mmol) was added to dry tetrahydrofuran (3 ml), and a butyllithium solution (3.9 ml, 6.2 mmol) in hexane was added dropwise at -40° C., the miXture was kept at -10° C. for 1 hour. A solution of 3-methyl-2-(3-pyridyl)thiazolidin-4-one (1 g, 5.2 mmol) in dry tetrahydrofuran (7 ml) was added dropwise to the mixture at -20° to -10° C. After this reaction mixture had been kept between those temperatures for 1 hour, there were added at -10° C. 1 bromobutane (0.78 g, 5.7 mmol) dissolved in tetrahydrofuran (2 ml), sodium iodide (0.77 g, 5.2 mmol), and hexamethylphosphorotriamide (1 ml). This reaction mixture was kept at room temperature for 2 hours. The resulting mixture, after addition of a phosphate buffer (pH 7.0), was extracted with ethyl acetate. The extract was dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated by evaporation under reduced pressure. The residue was chromatographed on silica gel (hexane-ethyl acetate), giving 5-butyl-3-methyl-2-(3-pyridyl)thiazolidin-4-one (250 mg, 20% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021435
Source datasetuspto-grants-1991_06
ORD IDord-876df298e0df48f3b2adb74634501c21
Source noteuspto-grants-1991_06