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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807840Generated: October 27, 2026

Acetonitrile → methyl 4-(2-cyclopentyl-1H-imidazol-1-yl)-2-methyl-5-nitrobenzoate

https://huagongshe.com/reaction/1807840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-Cyclopentyl-1H-imidazoleHCID 15088613—
ReactantMethyl 4-fluoro-2-methyl-5-nitrobenzoateHCID 51342041—
ReactantMethyl 4-fluoro-2-methyl-3-nitrobenzoateHCID 58575232—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
Productmethyl 4-(2-cyclopentyl-1H-imidazol-1-yl)-2-methyl-5-nitrobenzoateHCID 58575136—

Reaction Conditions

Temperature70 °C

Reaction Steps

To 2.74 g of a mixture of methyl 4-fluoro-2-methyl-5-nitrobenzoate and methyl 4-fluoro-2-methyl-3-nitrobenzoate, 1.75 g of 2-cyclopentyl-1H-imidazole, and 17.5 mL of acetonitrile, was added 4.9 mL of triethylamine, followed by stirring at 70° C. for 7 hours. To the reaction mixture were added water and ethyl acetate, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate, and then solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (normal hexane/ethyl acetate) to obtain 2.12 g of methyl 4-(2-cyclopentyl-1H-imidazol-1-yl)-2-methyl-5-nitrobenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357688B2
Source datasetuspto-grants-2013_01
ORD IDord-80db762bcda749ac84aaaf5365c39d6a
Source noteuspto-grants-2013_01