HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734628Generated: October 30, 2026
ethyl 4-(4-nitrophenyl)-1H-pyrrole-3-carboxylate → ethyl 4-(4-aminophenyl)-1H-pyrrole-3-carboxylate
https://huagongshe.com/reaction/734628
Participants
| Role | Name | HCID | Charge |
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| Reactant | ethyl 4-(4-nitrophenyl)-1H-pyrrole-3-carboxylate | HCID 53440113 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | ethyl 4-(4-aminophenyl)-1H-pyrrole-3-carboxylate | HCID 69064082 | 44.6% |
Reaction Steps
0.2 g (0.769 mmol) of ethyl 4-(4-nitrophenyl)-1H-pyrrole-3-carboxylate is added at a temperature in the region of 20° C. to a suspension of 0.02 g (0.188 mmol) of 10% palladium on carbon in 15 cm3 of methanol. After hydrogenating for 20 hours in an autoclave under 3 bar of hydrogen, at a temperature in the region of 25° C., the reaction mixture is filtered, the catalyst is rinsed with three times 5 cm3 of methanol and then the filtrate is concentrated to dryness under reduced pressure (2.7 kPa) to give a residue which is stirred in 10 cm3 of diethyl ether and then filtered and dried under reduced pressure (2.7 kPa) to give 0.079 g of ethyl 4-(4-aminophenyl)-1H-pyrrole-3-carboxylate, in the form of a brown solid; EI: m/z=230 (M+) base peak, m/z=202 (M-C2H4+), m/z=157 (M-C2H5O+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592365B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-4910756467224a459cb9a3536399b6cd |
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| Source note | uspto-grants-2009_09 |
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