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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251739Generated: October 30, 2026

Sodium hydride → Methyl 5-methyl-2-((2-nitrophenyl)amino)thiophene-3-carboxylate

https://huagongshe.com/reaction/2251739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantMethyl-2-amino-5-methyl-3-thiophenecarboxylateHCID 675878—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 5-methyl-2-((2-nitrophenyl)amino)thiophene-3-carboxylateHCID 19592005—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred suspension of sodium hydride (2 g) in dry tetrahydrofuran (25 mL) under a nitrogen atmosphere was added a solution of methyl 2-amino-5-methylthiophene-3-carboxy-late (4.8 g, 0.028 mol) and 2-fluoronitrobenzene (4.0 g, 0.025 mol) in dry tetrahydrofuran (30 mL). The mixture was stirred at 25° C. for 20 hours, poured onto ice and partitioned between 2N hydrochloric acid and ethyl acetate. The organic extracts were dried over magnesium sulfate, the solvent was evaporated under reduced pressure and the title compound purified by chromatography on silica gel, eluted with toluene, and crystallized from ethanol (4.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE040033E1
Source datasetuspto-grants-2008_01
ORD IDord-b198f773e3c240e597de2e3cee276590
Source noteuspto-grants-2008_01