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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280375Generated: October 30, 2026

Nitrogen → tert-Butyl 4-amino-3,3-difluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/2280375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactanttert-Butyl 4-(benzylamino)-3,3-difluoropiperidine-1-carboxylateHCID 66710726—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-amino-3,3-difluoropiperidine-1-carboxylateHCID 56932105—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), tert-butyl 4-(benzylamino)-3,3-difluoropiperidine-1-carboxylate (0.186 g, 0.57 mmol) was dissolved in MeOH (5 mL) and wet Pd/C 10% (50 mg) was added. The flask was purged with H2 gas and the reaction mixture stirred under an H2 atmosphere for 2 h at rt. The reaction mixture was filtered over celite and the cake was washed with MeOH and EA. The filtrate was concentrated under reduced pressure to give tert-butyl 4-amino-3,3-difluoropiperidine-1-carboxylate as a colorless oil. LC-MS-conditions 08: tR=0.49 min; [M-CH3+H]+=222.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139524B2
Source datasetuspto-grants-2015_09
ORD IDord-2aac53795fe049d684178aa48c838a19
Source noteuspto-grants-2015_09