HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327068Generated: October 25, 2026
Iodoethane → Methyl 5-acetyl-2-ethoxybenzoate
https://huagongshe.com/reaction/327068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-acetylsalicylate | HCID 85444 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Methyl 5-acetyl-2-ethoxybenzoate | HCID 18536574 | 89% |
Reaction Steps
Iodoethane (16.4 g, 0.105 mol) was added to a stirred mixture of 5-acetyl-2-hydroxybenzoic acid methyl ester (10 g, 51.5 mol) and anhydrous potassium carbonate (14.4 g, 0.104 mol) in 2-butanone (200 ml) and the resulting mixture heated under reflux for 3 days. The solvent was removed by evaporation under vacuum and the residue partitioned between water (100 ml) and ethyl acetate (100 ml). The aqueous phase was removed and extracted with further ethyl acetate (4×100 ml). The organic solutions were combined, dried (Na2SO4) and evaporated under vacuum. The residue was chromatographed on silica gel (130 g), using a methanol in dichloromethane elution gradient (0-1% methanol), to give the title compound as colourless crystals (10.15 g, 89%) m.p. 50°-55° C. Found C,64.88; H,6.38. C12H14O4 requires C,64.85; H,6.35%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05272147 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-56bf09700eed4f6ba5200807790a02e5 |
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| Source note | uspto-grants-1993_12 |
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