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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459719Generated: November 4, 2026

4-Fluorobenzylamine → tert-Butyl 4-((4-fluorobenzyl)amino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1459719

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzylamineHCID 67326—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Producttert-Butyl 4-((4-fluorobenzyl)amino)piperidine-1-carboxylateHCID 15380709—

Reaction Steps

4-Fluorobenzylamine (2.5 g) and N-tert-butoxycarbonyl-4-piperidone (4 g) were reacted as described in Example 98 (step 2), to give the title product as a yellow oil which crystallised (6.2 g). δH (250 MHz, CDCl3) 1.22-1.37 (2H, m), 1.43 (9H, s), 1.82-1.94 (2H, m), 2.60-2.72 (1H, m), 2.74-2.84 (2H, m), 3.80 (2H, s), 3.94-4.10 (2H, m), 6.97 (2H, m), 7.26-7.31 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854268
Source datasetuspto-grants-1998_12
ORD IDord-902ce0640b7849aab837c8ce451a8f98
Source noteuspto-grants-1998_12