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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588620Generated: October 31, 2026

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

https://huagongshe.com/reaction/588620

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 86717317352.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of ethyl 2-(5-acetamido-3-phenyl-pyrazol-1-yl)acetate (34.81 g, 60.6 mmol), iodic acid (5.33 g, 30.3 mmol) and iodine (15.37 g, 60.6 mmol) in ethanol (250 mL) was heated at 50° C. for 1.5 h and cooled to room temperature. The reaction mixture was concentrated in vacuo and the residue was dissolved in CH2Cl2 (250 mL). The solution was washed twice with 2 M Na2S2O3 followed by brine solution. The organic layer was dried (magnesium sulphate), filtered and concentrated in vacuo. The residue was triturated from diethyl ether, filtered and dried to provide the title compound as a solid (44.13 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227976B2
Source datasetuspto-grants-2016_01
ORD IDord-c523e6b814924de1aef1c9403ad4f6c5
Source noteuspto-grants-2016_01