HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219427Generated: October 30, 2026
Potassium Carbonate → Ethyl 4-[(3-cyanophenylamino)methyl]-3-nitrobenzoate
https://huagongshe.com/reaction/219427
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Aminobenzonitrile | HCID 16702 | — |
| Reactant | Ethyl 4-(bromomethyl)-3-nitrobenzoate | HCID 13685261 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 4-[(3-cyanophenylamino)methyl]-3-nitrobenzoate | HCID 18001123 | 54.9% |
Reaction Steps
Ethyl 4-bromomethyl-3-nitrobenzoate (26.00 g) was dissolved in 90 ml of acetonitrile, then 7.97 g of 3-aminobenzonitrile and 12.44 g of potassium carbonate were added and the mixture was stirred at 70° C. for 3 hours. The reaction solution was cooled to room temperature, and after filtration, the mother liquor was concentrated in vacuo. Ethyl acetate was added to the resulting residue. The mixture was washed with a 1N aqueous solution of hydrochloric acid and a saturated aqueous solution of sodium bicarbonate, dried over anhydrous magnesium sulfate and concentrated in vacuo. The resulting residue was purified by silica gel column chromatography using hexane-ethyl acetate (80:20 to 75:25) as an eluting solvent to give 12.06 g of ethyl 4-[(3-cyanophenylamino)methyl]-3-nitrobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE043481E1 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-3ff203a00ad242f3ab6d0fc405be7f61 |
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| Source note | uspto-grants-2012_06 |
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