Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
ReactantMethyl 2,2-difluoro-2-(fluorosulfonyl)acetateHCID 547667—
ReactantMethyl 4-bromo-5-iodothiophene-2-carboxylateHCID 57826852—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDmf hmpaHCID 19433458—
ProductMethyl 4-bromo-5-(trifluoromethyl)thiophene-2-carboxylateHCID 57826561197%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410158B2
Source datasetuspto-grants-2013_04
ORD IDord-6c7e44521c894e1a9b4ecdd59f8237c9
Source noteuspto-grants-2013_04