HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504576Generated: October 29, 2026
Dimethylformamide → Methyl 4-(trifluoromethyl)-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/1504576
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | 2-Fluoro-6-(trifluoromethyl)benzaldehyde | HCID 521933 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 4-(trifluoromethyl)-1-benzothiophene-2-carboxylate | HCID 18526201 | 35.4% |
Reaction Steps
A mixture of 1.00 g of 2-fluoro-6-(trifluoromethyl)benzaldehyde, 633 mg of methyl thioglycolate, 1.21 g of potassium carbonate and 15 ml of DMF was stirred at 130° 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 480 mg of methyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate (present condensed ring compound 3).
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-049c933fb52e49a58938bbb9be9b27a1 |
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| Source note | uspto-grants-2015_12 |
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