Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862039Generated: October 29, 2026

Water → 2-Benzyl-3-(p-nitrophenyl)propionic acid

https://huagongshe.com/reaction/862039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantDiethyl benzyl-4-nitrobenzylmalonateHCID 53932722—
SolventEthanolHCID 702—
Product2-Benzyl-3-(p-nitrophenyl)propionic acidHCID 2184825759.1%

Reaction Steps

A mixture of diethyl benzyl-4-nitrobenzylmalonate (24 g), KOH (14 g) and water (100 ml)-ethanol (150 ml) was stirred at 90°-100° C. for 7 hours. The reaction mixture was concentrated under reduced pressure and the residue was acidified with 1N HCl and extracted with ethylacetate. The ethyl acetate layer was washed with brine, dried (MgSO4) and concentrated under reduced pressure. The residue was dissolved in pyridine (100 ml) and the solution was stirred at 90° C. for 16 hours. The organic solvent was evaporated off and the residue was acidified with 1N HCl and extracted with ethyl acetate. The ethyl acetate layer was washed with brine, dried (MgSO4) and concentrated under reduced pressure. The residual oil was purified by column chromatography on silica gel. Elution with ethyl acetate-hexane (1:3, v/v) gave 2-benzyl-3-(p-nitrophenyl)propionic acid (10.5 g, 59%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716980
Source datasetuspto-grants-1998_02
ORD IDord-58ba6463b2e14894821d5965ef93a354
Source noteuspto-grants-1998_02