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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339704Generated: October 25, 2026

Tert-butyl 4-(benzylamino)-3-fluoropiperidine-1-carboxylate → 1,1-Dimethylethyl (3R,4S)-4-amino-3-fluoro-1-piperidinecarboxylate

https://huagongshe.com/reaction/339704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(benzylamino)-3-fluoropiperidine-1-carboxylateHCID 21948938—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product1,1-Dimethylethyl (3R,4S)-4-amino-3-fluoro-1-piperidinecarboxylateHCID 1126443597.4%

Reaction Steps

To a 250 mL glass Parr vessel was added the product from Step C (14.8 g, 48.0 mmol) and EtOH (100 mL). Pearlman's Catalyst (4.72 g, 3.36 mmol) was added and the mixture was shaken in a Parr reactor under 40-45 psi H2 for 15 hours. The reaction was filtered through celite and the celite was washed with EtOAc. The filtrate was concentrated and the residue was dissolved in CH2Cl2 and filtered through celite, and the celite was washed with CH2Cl2 and EtOAc. The filtrate was concentrated to afford 10.2 g (92%) of the desired product as a thick oil that slowly solidified to a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895550B2
Source datasetuspto-grants-2014_11
ORD IDord-af232c0af60544f6835140272ae9d548
Source noteuspto-grants-2014_11