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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Iodic acid | HCID 24345 | — |
| Reactant | ethyl 2-(5-acetamido-3-phenyl-1H-pyrazol-1-yl)acetate | HCID 86717316 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 2-(5-acetamido-4-iodo-3-phenyl-1H-pyrazol-1-yl)acetate | HCID 86717317 | 352.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227976B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-c523e6b814924de1aef1c9403ad4f6c5 |
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| Source note | uspto-grants-2016_01 |
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