HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271306Generated: October 30, 2026
Dimethylformamide → Methyl 7-(trifluoromethyl)-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/2271306
Participants
| Role | Name | HCID | Charge |
|---|
| 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 (the present compound 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09119396B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-02fd34350e7942eba74e894e4aac31d7 |
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| Source note | uspto-grants-2015_09 |
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