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
Participants
| Role | Name | HCID | Charge |
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| 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 | 325.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765762B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-215da535a12743e3b925e963b17b8da1 |
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| Source note | uspto-grants-2014_07 |
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