HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854721Generated: October 28, 2026
N-Iodosuccinimide → HCID 178517802, compound
https://huagongshe.com/reaction/1854721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 178515816 | HCID 178515816 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178517802 | HCID 178517802 | 83.2% |
Reaction Steps
NIS (7.38 g, 32.8 mmol) was added to a stirring solution of commercially available 5-bromo-6-chloropyridin-2-ol (5.70 g, 27.3 mmol) in MeOH (50 ml) at 45° C. The reaction was allowed to stir at 45° C. for 1 h. The amber colored solution was cooled to rt and then concentrated in vacuo. The resulting yellow solids were diluted with 25 mL DCM, triturated for 30 min, then collected filtering with minimal DCM to give 5-bromo-6-chloro-3-iodopyridin-2-ol (7.60 g, 22.7 mmol, 83% yield) as a white solid consistent by LCMS and NMR. LCMS: m/e 335 (M+H)+ LCMS retention time: 2.62 min. (Column: Phenomenex-Luna 50×2.0 mm 3u. Solvent A=90% Water: 10% Methanol: 0.1% TFA. Solvent B=10% Water: 90% Methanol: 0.1% TFA. Start % B=0. Final % B=100. Gradient Time=4 min. Flow Rate=0.8 mL/min.). 1H NMR (500 MHz, MeOD) δ ppm 8.26 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962651B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-7d496d7eb36c491dbe0ec15dc516c484 |
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| Source note | uspto-grants-2015_02 |
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