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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 4-(4-nitrophenyl)-1H-pyrrole-3-carboxylateHCID 53440113—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
Productethyl 4-(4-aminophenyl)-1H-pyrrole-3-carboxylateHCID 6906408244.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592365B2
Source datasetuspto-grants-2009_09
ORD IDord-4910756467224a459cb9a3536399b6cd
Source noteuspto-grants-2009_09