HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499691Generated: November 2, 2026
Iodoethane → 1-(5-Chloro-2-ethoxy-3-iodo-4-methylphenyl)ethanone
https://huagongshe.com/reaction/1499691
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(5-Chloro-2-hydroxy-3-iodo-4-methylphenyl)ethanone | HCID 11472394 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(5-Chloro-2-ethoxy-3-iodo-4-methylphenyl)ethanone | HCID 86666865 | 91.7% |
Reaction Steps
1-(5-Chloro-2-hydroxy-3-iodo-4-methylphenyl)ethanone (18.9 g, 60.9 mmol) (from Example 1, Step 1) was dissolved in N,N-dimethylformamide (60.8 mL). Iodoethane (7.3 mL, 91 mmol) was added followed by potassium carbonate (17 g, 120 mmol). The reaction was heated at 60° C. for 1 hour. The mixture was cooled to room temperature, diluted with ether. The organic layers were combined, washed with water, dried over MgSO4, concentrated and purified on silica gel (eluting with 0-10% EtOAc in hexanes) to give the desired product (18.9 g, 91.7%). LCMS calculated for C11H13ClIO2 (M+H)+: m/z=339.0; Found: 339.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199982B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-f4a9bd7c8c894782b8a337878300d3ad |
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| Source note | uspto-grants-2015_12 |
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