HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961285Generated: October 30, 2026
Potassium Fluoride → Methyl 4-bromo-5-(trifluoromethyl)thiophene-2-carboxylate
https://huagongshe.com/reaction/1961285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Methyl 2,2-difluoro-2-(fluorosulfonyl)acetate | HCID 547667 | — |
| Reactant | Methyl 4-bromo-5-iodothiophene-2-carboxylate | HCID 57826852 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dmf hmpa | HCID 19433458 | — |
| Product | Methyl 4-bromo-5-(trifluoromethyl)thiophene-2-carboxylate | HCID 57826561 | 197% |
Reaction Steps
To a solution of methyl 4-bromo-5-iodo-2-thiophenecarboxylate (500 mg, 1.44 mmol), copper (I) iodide (137 mg, 0.72 mmol) and potassium fluoride (251 mg, 4.32 mmol) in DMF/HMPA (5 ml/5 mL) was added methyl difluoro(fluorosulfonyl)acetate (1.1 g, 5.76 mmol). The mixture was heated at 70° C. under N2 in a sealed tube. After 1 h, the reaction was quenched with NH4Cl (sat'd) (2 mL), extracted with ether (5 mL×5) and washed with distilled water (5 mL×5). The combined organic phase was dried over Mg2SO4 and purified on silica (EtOAc/Hex, 20-50%) to afford the title compound (0.82 g) containing a 60% inseparable impurity: LC-MS m/z (ES) 290 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08410158B2 |
|---|
| Source dataset | uspto-grants-2013_04 |
|---|
| ORD ID | ord-6c7e44521c894e1a9b4ecdd59f8237c9 |
|---|
| Source note | uspto-grants-2013_04 |
|---|