HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504575Generated: October 30, 2026
Dimethylformamide → Methyl 6-(trifluoromethyl)-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/1504575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | 2-Fluoro-4-(trifluoromethyl)benzaldehyde | HCID 522929 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 6-(trifluoromethyl)-1-benzothiophene-2-carboxylate | HCID 18526202 | 56.4% |
Reaction Steps
A mixture of 1.11 g of 2-fluoro-4-(trifluoromethyl)benzaldehyde, 739 mg of methyl thioglycolate, 1.3 g of potassium carbonate and 20 ml of DMF was stirred at 140° C. for 2 hours. The reaction mixture was cooled down to room temperature. To the reaction mixture was added water, and the mixture was extracted with tert-butyl methyl ether three times. The combined organic layers were washed with water and saturated saline, and dried over magnesium sulfate, then, concentrated under reduced pressure, to obtain 848 mg of methyl 6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate (present condensed ring compound 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09215871B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-04402ee208c54390b135dee042494c2d |
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| Source note | uspto-grants-2015_12 |
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