HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877913Generated: October 29, 2026
N-Iodosuccinimide → HCID 178517797, compound
https://huagongshe.com/reaction/877913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2(1H)-Pyridinone, 3-(trifluoromethyl)- | HCID 3678411 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178517797 | HCID 178517797 | 81.9% |
Reaction Steps
3-trifluoromethyl-2-pyridinol (25 g, 153.3 mmol) is dissolved in anhydrous CH3CN (150 mL) and DMF (150 mL). N-iodosuccinimide (34.5 g, 153 mmol) is then added. The reaction mixture is stirred at 80° C. for 2 hours and cooled to room temperature. Aqueous 1 M NaHCO3 (150 mL) is then added to the cooled mixture. After stirring for 5 min, the solvents are evaporated to dryness. Water is added and the aqueous phase is extracted (×2) with dichloromethane. The organic phase is then evaporated and the desired product is recrystallized in water to afford 36.2 g (81%) of a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987452B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-4d4d028115a842858d6b89c6e040c15e |
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| Source note | uspto-grants-2015_03 |
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