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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615728Generated: October 31, 2026

Iodine → ethyl 2-(5-acetamido-4-iodo-3-phenyl-1H-pyrazol-1-yl)acetate

https://huagongshe.com/reaction/1615728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantIodic acidHCID 24345—
Reactantethyl 2-(5-acetamido-3-phenyl-1H-pyrazol-1-yl)acetateHCID 86717316—
SolventEthanolHCID 702—
Productethyl 2-(5-acetamido-4-iodo-3-phenyl-1H-pyrazol-1-yl)acetateHCID 86717317325.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of ethyl 2-(5-acetamido-3-phenyl-pyrazol-1-yl)acetate (37 g, 129 mmol), iodic acid (5.6 g, 32 mmol) and iodine (19.7 g, 77 mmol) in ethanol (400 mL) was heated at 50° C. for 2 h and cooled to room temperature. The reaction mixture was concentrated in vacuo and the residue was eluted through a pad of silica gel with CH2Cl2 diethyl ether (1:0 to 97:3). The residue was partitioned between CH2Cl2 and 2 M Na2S2O3 aq. solution. The layers were separated and the organic washed was dried (MgSO4), and concentrated in vacuo to provide a residue that was partially purified by chromatography (silica gel, CH2Cl2/isohexane 1:1 to 1:0, then CH2Cl2/diethyl ether 9:1 to 8:2), then triturated with diethyl ether to provide the title compound as an off-white solid (43 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765762B2
Source datasetuspto-grants-2014_07
ORD IDord-215da535a12743e3b925e963b17b8da1
Source noteuspto-grants-2014_07