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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Cyclopentyl-1H-imidazole | HCID 15088613 | — |
| Reactant | Methyl 4-fluoro-2-methyl-5-nitrobenzoate | HCID 51342041 | — |
| Reactant | Methyl 4-fluoro-2-methyl-3-nitrobenzoate | HCID 58575232 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl 4-(2-cyclopentyl-1H-imidazol-1-yl)-2-methyl-5-nitrobenzoate | HCID 58575136 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357688B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-80db762bcda749ac84aaaf5365c39d6a |
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| Source note | uspto-grants-2013_01 |
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