HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443694Generated: October 26, 2026
Methyl iodide → 1-(5-Chloro-2-methoxyphenyl)ethanone
https://huagongshe.com/reaction/1443694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-6-hydroxyacetophenone | HCID 74061 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(5-Chloro-2-methoxyphenyl)ethanone | HCID 240434 | 79.1% |
Reaction Steps
Dissolve 5′-chloro-2′-hydroxyacetophenone (15.3594 g, 90.03 mmol) in 100 mL of anhydrous acetonitrile in a pressure vessel. Add K2CO3 (13.7541 g, 99.52 mmol) and MeI (25.56 mL, 180.06 mmol) to the vessel. Seal the vessel and heat the reaction mixture to 85° C. for 18 hours. Cool the reaction and concentrate it in vacuo. Partition the residue between Et2O and H2O. Wash the organic layers with 2N NaOH (2×). Dry the combined organic layers with MgSO4. Filter off the drying agent and concentrate in vacuo to afford 13.15 g of 1-(5-chloro-2-methoxy-phenyl)-ethanone (79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662771B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-e324b1916b7542d6b15e3a4e10d4b8fd |
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| Source note | uspto-grants-2010_02 |
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