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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394292Generated: November 3, 2026

N-t-butoxycarbonyl-4-(4-fluorobenzylidene)piperidine → 4-(4-Fluoro-benzyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1394292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-t-butoxycarbonyl-4-(4-fluorobenzylidene)piperidineHCID 22676694—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product4-(4-Fluoro-benzyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 2267667984.3%

Reaction Steps

1-tert-Butoxycarbonyl-4-(4-fluorobenzylidene)piperidine (47.0 g) was dissolved in methanol (450 ml). To the solution was added 10% palladium carbon (water content: 50%, 4.7 g), and the mixture was subjected to catalytic hydrogenation reaction for 5 hours. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure to give 1-tert-butoxycarbonyl-4-(4-fluorobenzyl)piperidine (39.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348324B2
Source datasetuspto-grants-2008_03
ORD IDord-9b027a0af0a6494db26112c3c3d7572a
Source noteuspto-grants-2008_03