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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800810Generated: November 1, 2026

Tert-butyl 4-cyano-4-phenylpiperidine-1-carboxylate → Tert-butyl 4-(aminomethyl)-4-phenylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1800810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-cyano-4-phenylpiperidine-1-carboxylateHCID 10708369—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventAcetic acid ethanolHCID 18476134—
ProductTert-butyl 4-(aminomethyl)-4-phenylpiperidine-1-carboxylateHCID 1056545232%

Reaction Steps

Tert-butyl 4-cyano-4-phenylpiperidine-1-carboxylate (2.6 g, 9.08 mmol) was dissolved in 15% acetic acid/ethanol and hydrogenated at 50 psi over platinum oxide (0.052 g) for a week. HPLC showed only 50% conversion and the reaction was resubmitted to the same conditions and hydrogenated for 4 more days. The reaction was then filtered and the filtrate was evaporated. The residue was diluted with ethyl acetate and 1N hydrochloric acid. The aqueous phase was collected, basified with sodium carbonate and extracted with ethyl acetate. The combined organic phases were dried over anhydrous magnesium sulfate, filtered and concentrated to give the title material (0.835 g, 32%) as an oil which was used as such for the next reaction. LC/MS (M-(t-Bu)+H)+: 235. HPLC ret. time (Condition B): 1.322 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343999B2
Source datasetuspto-grants-2013_01
ORD IDord-3169c6071a4e4990a142bbb95ba9cf79
Source noteuspto-grants-2013_01