Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063313Generated: October 29, 2026

HCID 69019899, compound → 4-(Boc-aMino)-3,3-diMethylpiperidine

https://huagongshe.com/reaction/1063313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69019899HCID 69019899—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(Boc-aMino)-3,3-diMethylpiperidineHCID 1017139099.4%

Reaction Steps

(+)-1-Benzyloxycarbonyl-4-t−butyloxycarbonylamino-3,3-dimethylpiperidine (75 g, 0.207 mol) was dissolved in 500 ml methanol and the solution was transferred to a Parr reactor. Wet 10% palladium on carbon (7.5 g) was added to the solution and was stirred at 200 psi hydrogen pressure. Reaction progress was monitored on TLC and reaction was completed in 3-4 hrs. The reaction mixture was filtered as soon as it was completed. The residue was washed with 100 ml methanol. Fitrate was evaporated to dryness to afford the required product (47 g) in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964966B2
Source datasetuspto-grants-2005_11
ORD IDord-a9c3206955a140a8a80d81f5c9e03d5a
Source noteuspto-grants-2005_11