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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364051Generated: November 1, 2026

Dimethylformamide → Methyl 5-bromo-3-[(2,2-difluoroethyl)amino]thiophene-2-carboxylate

https://huagongshe.com/reaction/2364051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant2,2-Difluoroethyl trifluoromethanesulfonateHCID 2774089—
ReactantMethyl 5-bromo-3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylateHCID 56965789—
SolventWaterHCID 962—
ProductMethyl 5-bromo-3-[(2,2-difluoroethyl)amino]thiophene-2-carboxylateHCID 8666229764%

Reaction Steps

A mixture of methyl 5-bromo-3-[(trifluoroacetyl)amino]thiophene-2-carboxylate (500 mg, 1.51 mmol), 2,2-difluoroethyl trifluoromethanesulfonate (441 mg, 2.06 mmol), cesium carbonate (1.23 g, 3.78 mmol) and DMF (10 mL) was microwave-irradiated at 90° C. for 1 h. Then, water was added to quench the reaction. The organic materials were extracted with EtOAc. The combined extracts were washed with water and brine, dried over Na2SO4 and filtered. After removal of the solvent at reduced pressure, the residue was dissolved in MeOH (3 mL). To the solution were added potassium carbonate (100 mg) and water (1.5 mL). The mixture was stirred at room temperature for 0.5 h. After removal of the solvent at reduced pressure, the organic materials were extracted with EtOAc. The combined extracts were washed with brine, dried over Na2SO4 and filtered. After removal of the solvent at reduced pressure, the residue was purified by column chromatography (Purif, silica gel, hexane to 85:15 hexane/EtOAc) to give the title compound (290 mg, 64%) as a yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691828B2
Source datasetuspto-grants-2014_04
ORD IDord-5665869e23b046ee8d43b13335580285
Source noteuspto-grants-2014_04