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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512480Generated: November 1, 2026

Ethyl 1-(4-nitro-3-(2,2,2-trifluoroethoxy)phenyl)cyclobutanecarboxylate → Ethyl 1-(4-amino-3-(2,2,2-trifluoroethoxy)phenyl)cyclobutanecarboxylate

https://huagongshe.com/reaction/1512480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-(4-nitro-3-(2,2,2-trifluoroethoxy)phenyl)cyclobutanecarboxylateHCID 57995578—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductEthyl 1-(4-amino-3-(2,2,2-trifluoroethoxy)phenyl)cyclobutanecarboxylateHCID 5799564797.3%

Reaction Steps

To a stirred solution of ethyl 1-(4-nitro-3-(2,2,2-trifluoroethoxy)phenyl)cyclobutanecarboxylate (900 mg), in dry MeOH (50 mL), Pd(OH)2 (400 mg) was added and the mixture reduced under an atmosphere of H2 for 6 h at room temperature. The mixture was filtered through a pad of Celite™ washing with MeOH, the combined filtrates were concentrated under reduced pressure to yield ethyl 1-(4-amino-3-(2,2,2-trifluoroethoxy)phenyl)cyclobutanecarboxylate (800 mg) as a thick liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217064B2
Source datasetuspto-grants-2012_07
ORD IDord-21134240e4f14550b8a5963a7a90d263
Source noteuspto-grants-2012_07