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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045720Generated: October 30, 2026

Hydrochloric Acid → Ethyl 4-methyl-3-(2-nitrophenyl)-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/2045720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantEthyl isocyanoacetateHCID 533707—
Reactant1-Nitro-2-(2-nitroprop-1-en-1-yl)benzeneHCID 2731316—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 4-methyl-3-(2-nitrophenyl)-1H-pyrrole-2-carboxylateHCID 1592618959.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 1-nitro-2-[2-nitroprop-1-en-1-yl]benzene (4.1 g, 19.7 mmol) in a mixture of THF (131 mL) and tert-BuOH (66 mL) was treated with DBU (4.45 mL, 29.5 mmol) and ethyl isocyanoacetate (2.67 g, 2.58 mL) added. The resulting solution was stirred for 1 h, then heated to 70° C. for 4 h. The mixture was cooled and concentrated in vacuo to give residue that was taken up in EtOAc and aqueous HCl (1 N). The organic layer was separated and washed with brine, then dried over Na2SO4. Filtration and solvent removal afforded a residue that was purified on silica gel (gradient elution, 0-40% EtOAc/hexanes) to afford the title compound (3.2 g, 59%) as solid. LCMS (ES+) m/z 275 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08591878B2
Source datasetuspto-grants-2013_11
ORD IDord-62377b6b61dd4a039e40b89cb95e3ddc
Source noteuspto-grants-2013_11