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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377082Generated: October 31, 2026

Ethyl 4-(4-nitrophenyl)-4-oxobutanoate → ethyl 4-(4-aminophenyl)-4-oxobutanoate

https://huagongshe.com/reaction/1377082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-(4-nitrophenyl)-4-oxobutanoateHCID 15535281—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Productethyl 4-(4-aminophenyl)-4-oxobutanoateHCID 23233830.7%

Reaction Steps

A solution of ethyl 4-(4-nitrophenyl)-4-oxobutyrate (1.4 g, 5.6 mmol) and 10% palladium on carbon (0.18 g) in ethanol (50 ml) was shaken under hydrogen (50 psi) for 2 hours then filtered and concentrated in vacuo. The residue was absorbed onto silica gel (5 g) from an ethyl acetate solution and purified by chromatography on silica gel (100 g) eluting with ethyl acetate:hexane (1:2) to give ethyl 4-(4-aminophenyl)-4-oxobutyrate (0.38 g) as a white solid. 1H NMR (DMSO-d6, 300 MHz) δ: 1.17 (t, J=7 Hz, 3H, CH3), 2.56 (t, J=6.5 Hz, 2H, CH2), 3.10 (t, J=6.5 Hz, 2H, CH2), 4.04 (q, J=7 Hz, 2H, ester CH2), 6.04 (br s, 2H, NH2), 6.57 (d, J=9 Hz, 2H, Ar), 7.69 (d, J=9 Hz, 2H, Ar). Anal. Calculated for C12H15NO3 : C, 65.14; H, 6.83; N, 6.33. Found: C, 65.23; H, 6.85; N, 6.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663337
Source datasetuspto-grants-1997_09
ORD IDord-ad1c8349ad7243d1b3f43794f7b3d1f9
Source noteuspto-grants-1997_09