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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353952Generated: October 30, 2026

Ammonia → tert-Butyl 4-amino-4-cyanopiperidine-1-carboxylate

https://huagongshe.com/reaction/353952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantSodium CyanideHCID 8929—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Producttert-Butyl 4-amino-4-cyanopiperidine-1-carboxylateHCID 22091429—

Reaction Steps

t-Butyl 4-oxo-1-piperidine-carboxylate (10 g, 50 mmol, 1.0 equiv) was dissolved 100 mL of 2 M NH3 in MeOH. NaCN (2.7 g, 55 mmol, 1.1 equiv) and NH4Cl (3 g, 55 mmol, 1.1 equiv) were added and the resulting mixture was refluxed for 2 h at which time an additional 100 mL of 2 M NH3 in MeOH was added followed by another 2 h of reflux. The reaction mixture was cooled and filtered. The MeOH was removed in vacuo and the residue triturated with 100 mL of CH2Cl2 and filtered again. The filtrate was concentrated by about 75% and 200 mL of hexanes was added to give a tan precipitate that was collected by filtration to yield, after drying under vacuum, the desired product as cream-colored solid (10.1 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756372B2
Source datasetuspto-grants-2004_06
ORD IDord-2330fa9fb45a4dd88d5ae5392f5bb6e7
Source noteuspto-grants-2004_06