HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589281Generated: October 30, 2026
Dimethylformamide → Methyl 6-(trifluoromethyl)-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/589281
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 hours, and then 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 848 mg of methyl 6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09232792B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-0247623088074d76875e4ab95f35e7c3 |
|---|
| Source note | uspto-grants-2016_01 |
|---|