HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175700Generated: November 1, 2026
Potassium Carbonate → Methyl 5,6-dimethoxy-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/2175700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | 2-Fluoro-4,5-dimethoxybenzaldehyde | HCID 603595 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5,6-dimethoxy-1-benzothiophene-2-carboxylate | HCID 12521858 | 67% |
Reaction Steps
To a stirred solution of 2-fluoro-4,5-dimethoxybenzaldehyde (1.10 g, 6 mmol) in DMF (50 mL) was added methyl 2-mercaptoacetate (0.58 mL, 6.6 mmol) and potassium carbonate (2.48 g, 18 mmol). The resulting mixture was then heated at 60° C. for 15 hours. The DMF was removed via rotary evaporation and the residue was diluted with water and extracted with DCM. The organic phase was dried over sodium sulfate and the solvent was removed under reduced pressure to afford methyl 5,6-dimethoxybenzo[b]thiophene-2-carboxylate as a light yellow solid (1.0 g, 67%). LC-MS (ES-API); rt 8.48 min; m/z calculated for C12H12O4S [M+Na]+ 275.0, found 275.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062076B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-6c378ed51af043e88ec30e138ede6ecd |
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| Source note | uspto-grants-2015_06 |
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