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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483968Generated: October 25, 2026

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

https://huagongshe.com/reaction/483968

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-carboxylate (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 sulphate, the solvent was evaporated under reduced pressure and the title compound purified by chromatography on silica gel, eluted with toluene, and crystallised from ethanol (4.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229382
Source datasetuspto-grants-1993_07
ORD IDord-308d214c725e4e9d8c68673f1534a0a4
Source noteuspto-grants-1993_07