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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800827Generated: November 2, 2026

Tert-butyl 4-(aminomethyl)-4-phenylpiperidine-1-carboxylate → HCID 18318102, compound

https://huagongshe.com/reaction/1800827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(aminomethyl)-4-phenylpiperidine-1-carboxylateHCID 10565452—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
ProductHCID 18318102HCID 1831810264.7%

Reaction Steps

Tert-butyl 4-(aminomethyl)-4-phenylpiperidine-1-carboxylate (355 mg, 1.22 mmol) and 1.15 g PtO2 (5.1 mmol) in 125 ml ethanol were shaked in PARR apparatus under 60 psi of hydrogen for 20 hours. Celite was loaded on top of an ion exchange cartridge (MCX, Phenomenex, 6 g adsorbent). The crude reaction slurry was filtered through this set-up, the pyrophoric catalyst washed with ethanol and water and removed. The cartridge was washed with methanol and then the product eluted with a 2 M solution of NH3 in MeOH. The eluent was concentrated to give 234 mg of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343999B2
Source datasetuspto-grants-2013_01
ORD IDord-79b65f2b752143eeac49119228007a59
Source noteuspto-grants-2013_01