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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800825Generated: November 2, 2026

HCID 59321452, compound → Tert-butyl 4-(aminomethyl)-4-(2,3-dichlorophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1800825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59321452HCID 59321452—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
ProductTert-butyl 4-(aminomethyl)-4-(2,3-dichlorophenyl)piperidine-1-carboxylateHCID 59321370—

Reaction Steps

Tert-butyl 4-cyano-4-(2,3-dichlorophenyl)piperidine-1-carboxylate (2.30 g, 6.47 mmol) was dissolved in 75 ml of a 7M solution of NH3 in MeOH. Raney Nickel (˜2 g aq. suspension) was added and the mixture shaken on a PARR apparatus under 60 psi of hydrogen for 4 days. The catalyst was removed by filtration through a layer of Celite and the crude reaction mixture concentrated. The crude product (1.90 g yellow oil) was used in the next reaction (amide bond formation) “as is”.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343999B2
Source datasetuspto-grants-2013_01
ORD IDord-c74be3264331470aaac52b37e03979e6
Source noteuspto-grants-2013_01