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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854721Generated: October 28, 2026

N-Iodosuccinimide → HCID 178517802, compound

https://huagongshe.com/reaction/1854721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 178515816HCID 178515816—
SolventMethanolHCID 887—
ProductHCID 178517802HCID 17851780283.2%

Reaction Conditions

Temperature45 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962651B2
Source datasetuspto-grants-2015_02
ORD IDord-7d496d7eb36c491dbe0ec15dc516c484
Source noteuspto-grants-2015_02