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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515308Generated: October 29, 2026

tert-Butyl 4-(2,5-difluoro-4-nitrobenzylidene)piperidine-1-carboxylate → Tert-butyl 4-(4-amino-2,5-difluorobenzyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/515308

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(2,5-difluoro-4-nitrobenzylidene)piperidine-1-carboxylateHCID 67193923—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(4-amino-2,5-difluorobenzyl)piperidine-1-carboxylateHCID 67194990—

Reaction Steps

A mixture of tert-butyl 4-(2,5-difluoro-4-nitrobenzylidene)piperidine-1-carboxylate (4.52 mmol, 1.6 g) and palladium on carbon (10%) (0.135 mmol, 0.144 g) in ethyl acetate was hydrogenated at 3 bar until the desired amount of hydrogen was consumed. The reaction was filtered through celite and concentrated under reduced pressure to give the intermediate tert-butyl 4-(4-amino-2,5-difluorobenzyl)piperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108939B2
Source datasetuspto-grants-2015_08
ORD IDord-f03a9e7aa5394e5bae49c3767c369da8
Source noteuspto-grants-2015_08