HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177254Generated: November 2, 2026
Potassium Carbonate → Ethyl 4-hydroxy-2-methylbenzofuran-6-carboxylate
https://huagongshe.com/reaction/1177254
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Benzofurancarboxylic acid, 4-(acetyloxy)-2-methyl-, ethyl ester | HCID 59560094 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-hydroxy-2-methylbenzofuran-6-carboxylate | HCID 11514065 | 95% |
Reaction Steps
A mixture of ethyl 4-(acetyloxy)-2-methyl-1-benzofuran-6-carboxylate in absolute ethanol (500 mL) and potassium carbonate (18 g, 0.13 mol) was stirred for 3 h at 60° C. The mixture was diluted with 500 mL of dichloromethane and the suspension was filtered. The precipitate was washed with 200 mL of dichloromethane. The combined solutions was washed with 200 mL of a 10% aqueous solution of citric acid and evaporated in vacuum to dryness. The crude product introduced into a silica gel column and eluted with hexane/ethyl acetate mixture (2:1) to give 20 g (91 mmol, 95%) of desired compound as a yellow solid. 1HNMR (DMSO d-6): 1.30 (t, H), 2.45 (s, 3H), 4.30 (qt, 2H), 6.65 (s, 1H), 7.28 (2, 1H), 7.53 (s, 1H), 10.25 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842713B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-34bdaca5a55c4d549bcc071f5300e895 |
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| Source note | uspto-grants-2010_11 |
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