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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727160Generated: November 4, 2026

4-Benzyl-3-[3-(4-benzyloxy-3-cyclopentyloxyphenyl)-4-nitrobutyryl]-oxazolidin-2-one → 4-(4-Benzyloxy-3-cyclopentyloxyphenyl)pyrrolidin-2-one

https://huagongshe.com/reaction/1727160

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyl-3-[3-(4-benzyloxy-3-cyclopentyloxyphenyl)-4-nitrobutyryl]-oxazolidin-2-oneHCID 68828432—
CatalystNickelHCID 935—
SolventEthyl AcetateHCID 8857—
Product4-(4-Benzyloxy-3-cyclopentyloxyphenyl)pyrrolidin-2-oneHCID 6883008688%

Reaction Conditions

Temperature50 °C

Reaction Steps

Nitro-compound 16 (4 g) was partially dissolved in 75 mL EtOAc/75 mL EtOH/75 mL dioxane, and a suspension of Raney Ni was added. The mixture was flushed with H2 three times. The mixture was stirred under H2 at 50° C. overnight, then filtered through celite. Concentration and chromatography of the residue on silica gel gave 2.2 g of the desired product. Yield: 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495016B2
Source datasetuspto-grants-2009_02
ORD IDord-af10b9769660490d9cef1b03d813bfc7
Source noteuspto-grants-2009_02