HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521438Generated: October 31, 2026
Iodoethane → Ethyl 4-ethoxy-3-hydroxybenzoate
https://huagongshe.com/reaction/521438
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3,4-Dihydroxybenzoate | HCID 77547 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-ethoxy-3-hydroxybenzoate | HCID 11106619 | — |
Reaction Steps
3,4-Dihydroxybenzoic acid ethyl ester (3.00 g, 16.0 mmol) was suspended in DMF (10 ml), potassium carbonate (2.21 g, 16.0 mmol) was added, the mixture was stirred for 5 min at room temperature, and then iodoethane (2.49 g, 16.0 mmol) was added. The mixture was stirred overnight, the addition of potassium carbonate and of iodoethane was repeated, and the mixture was stirred overnight again. The mixture was partitioned between 2 N hydrochloric acid and EA, the aqueous phase extracted with EA, and the combined organic extracts were washed with a saturated sodium hydrogencarbonate solution and a saturated sodium chloride solution, dried over sodium sulfate, filtered, and evaporated to dryness. The residue was purified by silica gel chromatography (HEP/EA gradient).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328071B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-04fe2bd3fdd241608a368826546293b5 |
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| Source note | uspto-grants-2016_05 |
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