HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589285Generated: October 25, 2026
Dimethylformamide → Methyl 7-(trifluoromethyl)-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/589285
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-3-(trifluoromethyl)benzaldehyde | HCID 517978 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 7-(trifluoromethyl)-1-benzothiophene-2-carboxylate | HCID 18526203 | 89.9% |
Reaction Steps
A mixture of 1.10 g of 2-fluoro-3-(trifluoromethyl)benzaldehyde, 663 mg of methyl thioglycolate, 1.03 g of potassium carbonate and 15 ml of DMF was stirred at 60° 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 to obtain 1.34 g of methyl 7-(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-30253522c6a04abe8c78526891c5ee3a |
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| Source note | uspto-grants-2016_01 |
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