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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258693Generated: October 31, 2026

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

https://huagongshe.com/reaction/2258693

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, 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.I4; 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 numberUS05661155
Source datasetuspto-grants-1997_08
ORD IDord-299413afb7bc4b8c9c3b4f5952e2a021
Source noteuspto-grants-1997_08