Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615702Generated: October 31, 2026

Iodine → N-(4-iodo-1H-pyrazol-5-yl)acetamide

https://huagongshe.com/reaction/1615702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantIodic acidHCID 24345—
Reactant3-AcetylaminopyrazoleHCID 2777527—
SolventEthanolHCID 702—
ProductN-(4-iodo-1H-pyrazol-5-yl)acetamideHCID 86717260348.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of N-(1H-pyrazol-5-yl)acetamide (60 g, 0.48 mol), iodic acid (21.1 g, 0.12 mol) and iodine (61 g, 0.24 mol) in ethanol (1.6 L) was heated at 60° C. for 1.5 h and cooled to room temperature. The reaction mixture was concentrated in vacuo and partitioned between ethyl acetate and 2 M Na2S2O3 aq. solution. The layers were separated and the aqueous extracted with ethyl acetate. The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo to provide the title compound as a solid (105 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765762B2
Source datasetuspto-grants-2014_07
ORD IDord-d3d30bc4b9954565895fa88ee2f52698
Source noteuspto-grants-2014_07