HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643795Generated: November 1, 2026
Ethanol → ethyl 4-hydroxy-1-benzothiophene-6-carboxylate
https://huagongshe.com/reaction/1643795
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 86624768 | HCID 86624768 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 4-hydroxy-1-benzothiophene-6-carboxylate | HCID 11379055 | 37% |
Reaction Steps
4-(Acetyloxy)-1-benzothiophene-6-carboxylate was dissolved in absolute ethanol (200 mL). Potassium carbonate (14 g, 0.1 mol) was added. The reaction mixture was stirred for 3 h at 60° C. and diluted with 200 mL of dichloromethane. The suspension was filtered. The precipitate was washed by 100 mL of dichloromethane. The combined solutions were washed by 200 mL of a 10% aqueous solution of citric acid and evaporated in vacuum to dryness. The obtained crude product was chromatographed on a layer of silica gel (150×100 mm) with hexane/ethyl acetate mixture, 2:1 as eluent to give 6.5 g (29 mmol, 37%) of ethyl 4-hydroxy-1-benzothiophene-6-carboxylate as a cream-colored solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119624B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-ed8080ba02924d84a09440329127b8fd |
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| Source note | uspto-grants-2012_02 |
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