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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708190Generated: October 25, 2026

2,4,6-Trimethylpyridine → (4R)-N-(2-Nitrooxyethyl)-2-oxothiazolidine-4-carboxamide

https://huagongshe.com/reaction/1708190

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantNitronium tetrafluoroborateHCID 11073463—
Reactant(4R)-N-(2-Hydroxyethyl)-2-oxothiazolidine-4-carboxamideHCID 53943884—
SolventAcetonitrileHCID 6342—
Product(4R)-N-(2-Nitrooxyethyl)-2-oxothiazolidine-4-carboxamideHCID 985610113.9%

Reaction Steps

0.44 g of nitronium tetrafluoroborate and a solution of 0.41 g of 2,4,6-collidine in 20 ml of acetonitrile were added at a temperature of from -10° C. to 0° C. to 30 ml of acetonitrile, and the resulting mixture was stirred at the same temperature for 30 minutes. At the end of this time, 0.50 g of (4R)-N-(2-hydroxyethyl)-2-oxothiazolidine-4-carboxamide was added to the mixture, and the mixture was stirred at room temperature for 4 hours. The reaction mixture was then freed from the solvent by distillation under reduced pressure. The residue was mixed with ethyl acetate and insoluble materials were filtered off. The filtrate was concentrated by evaporation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, using ethyl acetate as the eluent. The pale yellow crystals thus obtained were recrystallized from ethyl acetate, to give 86 mg of the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356918
Source datasetuspto-grants-1994_10
ORD IDord-4377a5b977344fe6ba8cd0d85621ec80
Source noteuspto-grants-1994_10