HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643777Generated: October 31, 2026
Potassium Carbonate → Ethyl 7-hydroxy-2-methyl-1-benzothiophene-5-carboxylate
https://huagongshe.com/reaction/1643777
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 7-(Acetyloxy)-2-methyl-1-benzothiophene-5-carboxylate | HCID 59560166 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 7-hydroxy-2-methyl-1-benzothiophene-5-carboxylate | HCID 59560351 | 84% |
Reaction Steps
Ethyl 7-(acetyloxy)-2-methyl-1-benzothiophene-5-carboxylate was dissolved in absolute ethanol (500 mL). Potassium carbonate (18 g, 0.13 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 residue was crystallized from ether/hexane mixture (1:5) to give the desired product 10 g (42 mmol, 84%) as a cream solid. 1H NMR (DMSO-d6): δ ppm 1.30 (t, 3H), 2.50 (s, 3H), 4.30 (qt, 2H), 7.20 (s, 1H), 7.95(s, 1H), 7.85 (s, 1H); MS(APCl, pos): 237.1.
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-68adeafbf0ad42a788403b1b6249bf58 |
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| Source note | uspto-grants-2012_02 |
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