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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736922Generated: October 30, 2026

(R)-3-[(E)-3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-acryloyl]-4-benzyl-oxazolidin-2-one → (R)-3-[3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-propionyl]-4-benzyl-oxazolidin-2-one

https://huagongshe.com/reaction/736922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-3-[(E)-3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-acryloyl]-4-benzyl-oxazolidin-2-oneHCID 68592504—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product(R)-3-[3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-propionyl]-4-benzyl-oxazolidin-2-oneHCID 68590943—

Reaction Steps

A mixture of 23.7 g (55.8 mmol) of (R)-3-[(E)-3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-acryloyl]-4-benzyl-oxazolidin-2-one, 400 mL of MeOH and 5.0 g of Raney nickel was shaken for 2 h at RT and 3 bar of H2 in a Parr autoclave. The catalyst was suction filtered and the solvent removed i. vac. The desired product was obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595312B2
Source datasetuspto-grants-2009_09
ORD IDord-2fd596c9eefc404dbb89ae1d077921de
Source noteuspto-grants-2009_09