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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093628Generated: October 31, 2026

4-Hydroxy-3-nitro-5-[(1E)-prop-1-en-1-yl]benzonitrile → 3-Amino-4-hydroxy-5-propylbenzonitrile

https://huagongshe.com/reaction/2093628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-3-nitro-5-[(1E)-prop-1-en-1-yl]benzonitrileHCID 68785334—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product3-Amino-4-hydroxy-5-propylbenzonitrileHCID 6874145026%

Reaction Steps

To a solution of 1.78 g of 4-hydroxy-3-nitro-5-[(1E)-prop-1-en-1-yl]benzonitrile in ethyl acetate (10 ml) was added palladium on carbon (100 mg). This mixture was evacuated and flushed with hydrogen (via balloon) 10 times. The reaction was stirred at room temperature for 14 h under hydrogen. The mixture was then filtered through a plug of Celite, eluting with methanol. After concentration of the eluent in vacuo, the residue was further purified by column chromatography on a Biotage Horizon, eluting with 1 column volume of 100% hexanes followed by a gradient of 0-20% ethyl acetate in hexanes over 10 column volumes to provide the title compound (400 mg, 26%). Mass spectrum (ESI) 177.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445480B2
Source datasetuspto-grants-2013_05
ORD IDord-71ac7e3b36c5490995e3a321899867ed
Source noteuspto-grants-2013_05