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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Reactant | Nitronium tetrafluoroborate | HCID 11073463 | — |
| Reactant | (4R)-N-(2-Hydroxyethyl)-2-oxothiazolidine-4-carboxamide | HCID 53943884 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (4R)-N-(2-Nitrooxyethyl)-2-oxothiazolidine-4-carboxamide | HCID 9856101 | 13.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05356918 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-4377a5b977344fe6ba8cd0d85621ec80 |
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| Source note | uspto-grants-1994_10 |
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