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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884036Generated: October 30, 2026

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

https://huagongshe.com/reaction/1884036

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, esterCH2), 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 numberUS06762188B1
Source datasetuspto-grants-2004_07
ORD IDord-e38833aff2c741f4b85f0e217210bd29
Source noteuspto-grants-2004_07