HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589283Generated: October 27, 2026
Dimethylformamide → Methyl 4-(trifluoromethyl)-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/589283
Participants
| Role | Name | HCID | Charge |
|---|
| 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 to room temperature. To the reaction mixture was added water, and then extracted with tert-butyl methyl ether 3 times. The combined organic layer was washed with water, followed by saturated aqueous sodium chloride solution. The mixture was dried over magnesium sulfate, and then concentrated under reduced pressure obtain 480 mg of methyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09232792B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-3eecd179de074839a2f5d6da214e2a65 |
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| Source note | uspto-grants-2016_01 |
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