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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588595Generated: October 29, 2026

Iodine → N-(2-acetyl-4-iodo-5-phenyl-pyrazol-3-yl)acetamide

https://huagongshe.com/reaction/588595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantIodic acidHCID 24345—
ReactantN-(2-acetyl-5-phenyl-pyrazol-3-yl)acetamideHCID 86717295—
SolventEthanolHCID 702—
ProductN-(2-acetyl-4-iodo-5-phenyl-pyrazol-3-yl)acetamideHCID 86717296—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of N-(2-acetyl-5-phenyl-pyrazol-3-yl)acetamide (25.1 g, 0.103 mol), iodic acid (4.5 g, 0.026 mol) and iodine (15.7 g, 0.062 mol) in ethanol (250 mL) was heated at 50° C. for 3 h and cooled to room temperature. The reaction mixture was concentrated in vacuo and partitioned between CH2Cl2 and 2 M Na2S2O3 aq. solution. The layers were separated and the organic washed with brine, dried (phase separator cartridge), and concentrated in vacuo to provide a mixture of the title compound and starting material (2.2:1, 30.3 g). The mixture was put in reaction again using iodic acid (1.6 g, 9.6 mmol) and iodine (9.7 g, 0.038 mol) in ethanol (250 mL) under the same conditions, to provide the title compound as a solid (31.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227976B2
Source datasetuspto-grants-2016_01
ORD IDord-6240d929e3e247529e0946ed7bdb6529
Source noteuspto-grants-2016_01